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. 2026 Aug 25;18(8):e115189. doi: 10.7759/cureus.115189

Prescription Trends in the Management of Lower Urinary Tract Symptoms in Men: An Online Survey of Indian Urologists

Prakash Patwardhan 1, Santosh Palkar 2, Rahul Sharma 3, Sanjay Kamble 4,✉, Shubhra Dhurandhar 4
Editors: Alexander Muacevic, John R Adler
PMCID: PMC13614455  PMID: 42799232

Abstract

Background

Lower urinary tract symptoms (LUTS), highly prevalent among aging men, adversely affect the quality of life. Pharmacological management has evolved with multiple drug classes, but real-world prescribing patterns in India have not been adequately studied. Thus, we evaluated prescription trends among Indian urologists for the management of male LUTS, assessed symptom patterns, evaluated factors influencing choice of fixed-dose combination (FDC), with special focus on silodosin-mirabegron FDC, and identified adverse events (AEs) and adherence.

Methods

This cross-sectional, questionnaire-based survey was performed over three months (January 2, 2026, to April 5, 2026) and included 110 Indian urologists actively managing male patients with LUTS. A 27-item structured questionnaire captured demographic characteristics, clinical practice patterns, and prescribing preferences for LUTS pharmacotherapy, including monotherapies, combination therapies, and FDCs, along with AEs and adherence.

Results

Of 135 urologists invited, 110 (81.48%) completed the survey. LUTS mainly involved a combination of storage, voiding, and post-micturition symptoms (n = 59, 53.6%). As a class, α1-blockers were the most frequently prescribed monotherapy (n = 109, 99.1% frequent/very frequent use), with silodosin (n = 98, 89.1%) and tamsulosin (n = 84, 76.4%) being most preferred. Use of dutasteride (n = 108, 98.2%) exceeded finasteride (n = 13, 11.8%). In patients with benign prostatic hyperplasia (BPH) with overactive bladder, silodosin-mirabegron was the most favored FDC (n = 97, 88.2%). FDCs of α1-blockers with muscarinic receptor antagonists and β-3 adrenergic agonists were preferred due to their proven efficacies (n = 83, 75.5% and n = 87, 79.1%, respectively) and lower incidences of AEs (n = 69, 62.7% and n = 80, 72.7%). Common AEs included dry mouth (n = 73, 66.4%), anejaculation (n = 69, 62.7%), and headache (n = 67, 60.9%). Moderate adherence (25%-75%) was reported by 95 (86.4%) urologists.

Conclusion

Adherence to pharmacotherapy, as assessed by participating urologists, was moderate, with urologists preferring silodosin as first-line therapy and silodosin-mirabegron FDC for mixed LUTS.

Keywords: benign prostatic hyperplasia, fixed drug combination, lower urinary tract symptoms, muscarinic antagonists, practice patterns, α1-blockers

Introduction

Lower urinary tract symptoms (LUTS) include a range of symptoms, including storage, voiding, and post-micturition, which negatively affect quality of life (QoL) in aging men [1]. Globally, benign prostatic hyperplasia (BPH) remains the primary etiologic factor, with an estimated pooled prevalence of 26.2% [2], while overactive bladder (OAB) affects around 11.8% of men, increasing considerably with age [3]. India shares a significant burden, with community-based studies reporting LUTS suggestive of BPH in 10.3% of men aged 50 years or more, with age-specific prevalence increasing from 25% to over 50% in men aged 40-49 years to 70-79 years, respectively [4,5]. The most bothersome LUTS include nocturia, frequency, and urgency that interfere with routine activities, work productivity, and sleep [6].

Current guidelines from professional bodies, including the European Association of Urology (EAU) [7], American Urological Association (AUA) [8], Urological Society of India [9], and French LUTS Committee [10], recommend α1-blockers as first-line agents for moderate-to-severe LUTS, while 5α-reductase inhibitors (5-ARIs) are added when prostate volume exceeds 40 mL. Combination therapy involving α1-blockers and 5-ARIs reduces the risk of acute urinary retention by 81% compared to placebo, while 35% and 68% risk reduction were observed with doxazosin and finasteride, respectively [11]. Antimuscarinics or β-3 agonists (e.g., mirabegron) are recommended for predominant storage symptoms, while tadalafil is added in the presence of comorbid erectile dysfunction [7,10].

Despite the availability of various guidelines and their frequent updates, real-world prescription patterns vary substantially. Literature suggests low adherence to BPH pharmacotherapy, with one-year adherence rates ranging from 35% for α1-blockers to 9% for combination therapy with 5-ARIs [12]. Compared to separate tablets, use of fixed-dose combinations (FDCs) is reported to have significantly greater and longer duration of persistence [13]. However, such data remain scarce from low- and middle-income countries. A recent survey from India reported that silodosin is widely prescribed for BPH, especially in those with comorbidities, while mirabegron is used as a first-line therapy for managing OAB [14]. In spite of that, systematic evidence on prescribing trends, factors influencing selection of FDC, and adherence challenges in the context of Indian settings is lacking. Thus, the primary objective of the survey was to evaluate prescription trends among Indian urologists for the management of male LUTS. Meanwhile, the secondary objective was to evaluate symptom patterns and factors influencing choice of FDC and identify adverse events (AEs) as well as adherence challenges reported by participating urologists.

Materials and methods

Study design and ethics

This cross-sectional multiple-response online questionnaire-based survey was performed over a period of three months (January 2, 2026, to April 5, 2026). The study was approved by the Independent Ethics Committee (CIEC/2025/0408; dated December 29, 2025), and informed consent was obtained from urologists after explaining the purpose and benefits of the study.

Study population

The survey included 110 urologists across India who actively managed male patients with LUTS/BPH in their clinic, had at least two years of independent clinical practice post-residency/fellowship, and routinely managed and prescribed medication for a minimum of five new or existing male LUTS patients per month. Urologists were excluded if they treated fewer than five male LUTS/BPH patients per month, did not have prescribing authority for LUTS/BPH, and did not respond to the complete survey questionnaires.

Study procedure

A structured questionnaire was developed to evaluate the knowledge and practice of urologists associated with medical management of LUTS/BPH in men (Appendix). Questions were designed as multiple-choice to facilitate response standardization. The urologists prescribing medication for LUTS/BPH were recruited via convenience sampling from professional networks and their referrals and invited to take part in the survey. It was reviewed by two independent urologists for content and face validity, relevance, and clarity. However, as the questionnaire was designed for assessment of descriptive practice patterns without scoring or grading, it was not formally validated or pilot-tested. The urologists who accepted the invitation were briefed about the study details and asked to sign an informed consent form. After obtaining consent, the urologists were asked to complete an online questionnaire-based survey. This online questionnaire-based survey was conducted using Google Forms (Google, Mountain View, CA, USA), and only fully completed responses were included in the analysis. Upon completion of the survey, the response rate was calculated, and data were analyzed.

The survey collected demographic and professional information of urologists, including their sex, location of practice, and years of clinical practice. Moreover, information regarding presentation of patients with LUTS and their management, including frequency of managing men with LUTS, symptoms and etiologies of LUTS, pharmacological options preferred for managing these patients, drug(s) preferred within each available class, FDCs preferred in patients presenting with BPH and associated OAB, reasons for preferring FDC of muscarinic receptor antagonists (MRAs) and β-3 adrenergic agonists (mirabegron) for LUTS, and AEs, adherence, and feedback of patients regarding the tolerability of silodosin-mirabegron FDC, was collected.

Survey response rate

The survey response rate was determined by dividing the number of urologists who responded by the total number of urologists who participated. An 80% or greater response rate was taken into consideration for this survey [15]. Telephonic and in-person informed consent was obtained, and a questionnaire was sent to 135 urologists, of which 110 completed the survey, resulting in a response rate of 81.48%.

Statistical analyses

Due to the use of descriptive statistics, no inferential analyses were planned. Continuous variables were represented as mean values ± standard deviation (SD) or median values with range, while categorical variables were represented as percentages. Microsoft 365 Excel (Redmond, WA, USA) was used for performing descriptive analysis.

Results

All surveyed urologists were male (n = 110, 100%) and mainly practiced in non-metropolitan regions (n = 95, 86.4%). Most of the urologists had 5-10 years (n = 49, 44.5%) and 10-15 years (n = 34, 30.9%) of experience (Table 1).

Table 1. Demographic characteristics.

Data represented as frequency (percentage)

Characteristics n = 110 %
Sex, n (%)
Male 110 100
City of practice, n (%)
Metropolitan 15 13.6
Non-metropolitan 95 86.4
Years of clinical practice, n (%)
<5 years 9 8.2
5-10 years 49 44.5
10-15 years 34 30.9
15-20 years 9 8.2
>20 years 9 8.2

The majority of urologists reported that LUTS are very common in clinical practice (n = 76, 69.1%). The most frequently reported LUTS was a combination of storage, voiding, and post-micturition symptoms (n = 59, 53.6%), followed by mixed storage and voiding symptoms (n = 26, 23.6%). BPH with OAB (n = 56, 50.9%) and BPH alone (n = 25, 22.7%) were the most common etiologies of LUTS (Table 2).

Table 2. Clinical perspectives on prevalence, symptom patterns, and etiologies.

Data represented as frequency (percentage)

LUTS: lower urinary tract symptoms; BPH: benign prostatic hyperplasia; OAB: overactive bladder

Characteristics n = 110 %
How common is LUTS in men in clinical practice?
Not common 1 0.9
Common 33 30.0
Very common 76 69.1
Which LUTS are most frequently reported by men in clinical practice?
Storage symptoms 11 10.0
Voiding symptoms 13 11.8
Storage plus voiding symptoms 26 23.6
Voiding plus post-micturition symptoms 1 0.9
All of the above 59 53.7
What are the commonly attributed etiologies of LUTS in men observed in clinical practice?
BPH 25 22.7
BPH with OAB 56 50.9
BPH with bladder infections 3 2.7
BPH with OAB and bladder infections 8 7.3
BPH with OAB, bladder infections, and bladder pain syndrome 5 4.5
Bladder pain syndrome 1 0.9
OAB 6 5.6
OAB with bladder infections and bladder pain syndrome 3 2.7
Bladder infections and bladder pain syndrome 3 2.7

Of various pharmacological classes surveyed, α1-blockers were the most frequently prescribed monotherapy for men with LUTS, with nearly all urologists reporting very frequent (n = 77, 70.0%) or frequent (n = 32, 29.1%) use. Among other classes, 5-ARIs (n = 72, 65.5%), MRAs (n = 86, 78.2%), β-3 adrenergic agonists (n = 71, 64.5%), and phosphodiesterase 5 inhibitors (PDE5Is, n = 75, 68.2%) were frequently used, while selective serotonin and norepinephrine reuptake inhibitors (SNRIs) were less frequently (n = 40, 36.4%) and rarely (n = 41, 37.3%) used. Combination therapies of α1-blockers with 5-ARIs (n = 73, 66.4%), MRAs (n = 79, 71.8%), β-3 adrenergic agonists (n = 65, 59.1%), and PDE5Is (n = 69, 62.7%) were frequently used. Though the combination of β-3 agonists with MRAs was frequently used (n = 66, 60.0%), its combination with SNRIs was less frequently used (n = 48, 43.6%; Table 3).

Table 3. Prescribing patterns of pharmacological therapies.

Data represented as frequency (percentage)

5-ARIs: 5α-reductase inhibitors; MRAs: muscarinic receptor antagonists; PDE5Is: phosphodiesterase 5 inhibitors; SNRIs: serotonin and norepinephrine reuptake inhibitors; LUTS: lower urinary tract symptoms

Drug class Frequency of prescription (n = 110)
Very frequent Frequent Less frequent Rare
n % n % n % n %
How frequently are various pharmacological options preferred for men presenting with LUTS?  
α1-blockers 77 70.0 32 29.1 0 0.0 1 0.9
5-ARIs 28 25.4 72 65.5 10 9.1 0 0.0
PDE5Is 10 9.1 75 68.2 23 20.9 2 1.8
MRAs 14 12.7 86 78.2 10 9.1 0 0.0
β-3 adrenergic agonists 16 14.5 71 64.5 19 17.4 4 3.6
SNRIs 7 6.3 22 20.0 40 36.4 41 37.3
α1-blockers-5-ARIs 25 22.7 73 66.4 9 8.2 3 2.7
α1-blockers-MRAs 12 10.9 79 71.8 18 16.4 1 0.9
α1-blockers-β-3 adrenergic agonist 18 16.4 65 59.1 22 20.0 5 4.5
α1-blockers-PDE5Is 17 15.5 69 62.7 20 18.2 4 3.6
β-3 agonist-MRAs 18 16.3 66 60.0 19 17.3 7 6.4
β-3 agonist-SNRIs 7 6.4 31 28.2 48 43.6 24 21.8

Within drug classes, silodosin (n = 98, 89.1%) and tamsulosin (n = 84, 76.4%) were the most preferred α1-blockers, while, among 5-ARIs, dutasteride (n = 108, 98.2%) was overwhelmingly favored over finasteride (n = 13, 11.8%). Use of solifenacin (n = 103, 93.6%) dominated among MRAs, and mirabegron (n = 108, 98.2%) was the clear choice within β-3 adrenergic agonists. Tadalafil (n = 102, 92.7%) was strongly preferred over sildenafil (n = 11, 10.0%) among PDE5Is, and duloxetine (n = 107, 97.3%) was the predominantly used SNRI. Among FDCs for BPH with associated OAB, silodosin-mirabegron (n = 97, 88.2%) was the most favored (Table 4).

Table 4. Preferred drugs and fixed-dose combinations for management.

Data represented as frequency (percentage)

5-ARIs: 5α-reductase inhibitors; MRAs: muscarinic receptor antagonists; PDE5Is: phosphodiesterase 5 inhibitors; SNRIs: serotonin and norepinephrine reuptake inhibitors; LUTS: lower urinary tract symptoms; BPH: benign prostatic hyperplasia; OAB: overactive bladder

Drug class n = 110 %
Which drug(s) are preferred within each class for men presenting with LUTS in clinical practice?
α1-blockers
Tamsulosin 84 76.4
Silodosin 98 89.1
Alfuzosin 46 41.8
Terazosin 1 0.9
5-ARIs
Dutasteride 108 98.2
Finasteride 13 11.8
MRAs
Solifenacin 103 93.6
Fesoterodine 23 20.9
Darifenacin 17 15.5
Tolterodine 44 40.0
Oxybutynin 14 12.7
Trospium 5 4.5
Mirabegron 1 0.9
β-3 adrenergic agonists
Mirabegron 108 98.2
Vibegron 5 4.5
PDE5Is
Sildenafil 11 10.0
Tadalafil 102 92.7
SNRIs
Duloxetine 107 97.3
Venlafaxine 10 9.1
Dapoxetine 1 0.9
Which of the available fixed-dose combinations are preferred for patients presenting with BPH and associated OAB?
Silodosin-mirabegron 97 88.2
Silodosin-dutasteride 15 13.6
Alfuzosin-tadalafil 17 15.5
Alfuzosin-dutasteride 8 7.3
Alfuzosin-solifenacin 1 0.9
Tamsulosin-dutasteride 20 18.2
Tamsulosin-tadalafil 20 18.2
Tamsulosin-finasteride 2 1.8
Solifenacin-tamsulosin 1 0.9
Silodosin-dutasteride-mirabegron-solifenacin 1 0.9

Proven efficacy was the main reason for preferring both MRAs (n = 83, 75.5%) and β-3 adrenergic agonists (n = 87, 79.1%) in FDC regimens. A lower incidence of adverse effects was also a key factor, reported by 69 (62.7%) for MRAs and 80 (72.7%) for beta-3 agonists. Safety in patients with narrow-angle glaucoma or cognitive impairment influenced choice in 50 (45.5%) and 60 (54.5%) urologists, respectively (Table 5).

Table 5. Reasons for preference of muscarinic receptor antagonists and β-3 adrenergic agonists in fixed-dose combination regimens.

Data represented as frequency (percentage)

Characteristics n = 110 %
Muscarinic receptor antagonists
Cost-effective 24 21.8
Proven efficacy 83 75.5
Widely available 28 25.5
Failure of monotherapy 44 40.0
Safer in patients with narrow-angle glaucoma or cognitive impairment 50 45.5
Lesser incidence of adverse effects, including constipation and dry mouth 69 62.7
β-3 adrenergic agonists (mirabegron)
Cost-effective 22 20.0
Proven efficacy 87 79.1
Widely available 15 13.6
Failure of monotherapy 38 34.5
Safer in patients with narrow-angle glaucoma or cognitive impairment 60 54.5
Lesser incidence of adverse effects, including constipation and dry mouth 80 72.7

The most frequent AEs associated with the use of silodosin-mirabegron FDC were dry mouth (n = 73, 66.4%), anejaculation (n = 69, 62.7%), headache (n = 67, 60.9%), and dizziness (n = 52, 47.3%). Regarding adherence, 95 (86.4%) urologists reported that patients were moderately adherent to FDC (25%-75%). Despite AEs and moderate adherence, patient feedback was largely positive, with 51 (46.4%) urologists reporting a combination of improved QoL, reduced overall BPH-related symptoms, and good tolerability over an extended period, followed by a combination of improved QoL and reduced overall BPH-related symptoms (n = 37, 33.6%, Table 6).

Table 6. Tolerability, adherence, and patient-reported outcomes of combination therapy with silodosin and mirabegron.

Data represented as frequency (percentage)

LUTS: lower urinary tract symptoms; BPH: benign prostatic hyperplasia

Characteristics n = 110 %
Adverse events with combination therapy of silodosin and mirabegron
Dry mouth 73 66.4
Anejaculation 69 62.7
Headache 67 60.9
Dizziness 52 47.3
Postural hypotension 43 39.1
Nasal stuffiness 40 36.4
Constipation 37 33.6
Hypertension 32 29.1
Palpitation 16 14.5
Obstructed flow 12 10.9
Adherence to the combination therapy of silodosin and mirabegron
<25% patients 9 8.2
25%-50% patients 50 45.5
51%-75% patients 45 40.9
76%-100% patients 6 5.5
What is the feedback of patients with male LUTS regarding the tolerability of the combination therapy of silodosin and mirabegron compared to other combination therapies of muscarinic receptor antagonists?
Improved quality of life 14 12.7
Reduction in overall BPH-related symptoms 6 5.5
Good tolerability over an extended period 1 0.9
Improved quality of life + reduction in overall BPH-related symptoms 37 33.6
Reduction in overall BPH-related symptoms + good tolerability over an extended period 1 0.9
All of the above 51 46.4

Discussion

Among aging male populations, LUTS pose a significant clinical challenge, with considerable adverse impact on QoL [1]. Over a period of time, approval of various pharmacological classes, including α1-blockers, β-3 adrenergic agonists, 5-ARIs, MRAs, SNRIs, and PDE5Is, has led to substantial evolution in the management of male LUTS [8,10]. This survey provides an up-to-date understanding of real-world prescribing practices among Indian urologists, suggesting crucial trends that both align with and diverge from professional treatment guidelines.

The principal finding of this survey suggests that α1-blockers remain the foundation of LUTS pharmacotherapy, with 109 (99.1%) urologists confirming very frequent/frequent use. This is consistent with the EAU and the French LUTS Committee guidelines, which recommend α1-blockers as first-line therapy for men with moderate-to-severe LUTS [8,10]. The preference for silodosin (n = 98, 89.1%) over tamsulosin (n = 84, 76.4%) is a notable finding. This is consistent with the findings of an Indian expert survey, where 89.1% of specialists prescribe silodosin for BPH [16]. Being a highly selective α1A-blocker, silodosin is reported to have minimal vasodilatory properties, with a hypotensive effect identical to placebo [10]. Moreover, the selectivity of silodosin explains the lower incidence of cardiovascular AEs, though ejaculatory dysfunction remains a substantial consideration [10]. Meanwhile, a randomized controlled trial reported anejaculation rates of 73.9% with silodosin monotherapy, increasing to 84% when combined with mirabegron [17], attributed to differences in study population or pharmacodynamic interaction.

Among 5-ARIs, high preference for dutasteride (n = 108, 98.2%) over finasteride (n = 13, 11.8%) represents a significant shift from historical prescribing patterns. This finding is consistent with the available literature suggesting that dutasteride may lead to reduced risks of acute urinary retention and BPH-related surgery compared to finasteride [18]. Unlike finasteride, a selective type II 5-ARI, dutasteride inhibits both types I and II 5-ARIs and thus leads to nearly complete suppression of dihydrotestosterone (95%), likely describing its clinical preference despite comparable efficacy reported in the literature [10,19].

With reference to combination therapy of various classes, the frequent use of α1-blockers with MRAs (n = 79, 71.8%) and β-3 agonists (n = 65, 59.1%) suggests increasing awareness that storage symptoms usually dominate or persist even after adequate control of voiding symptoms [20]. A recent network meta-analysis concluded that combination therapies often show superior efficacy for urgency episodes and urge urinary incontinence than monotherapies [21]. The strong preference for mirabegron (n = 108, 98.2%) is consistent with the fact that mirabegron is widely used as a first-line treatment by Indian urologists [14]. Moreover, the efficacy of mirabegron is comparable to antimuscarinics without the risks of cognitive impairment, especially in elderly men [22].

High preference for silodosin-mirabegron FDC (n = 97, 88.2%) among surveyed urologists represents a unique finding. This is in agreement with the findings reported by another Indian survey that 82.5% of urologists preferred silodosin-mirabegron FDC [23]. This combination handles both components of mixed LUTS, with silodosin improving the voiding function by relaxing prostatic smooth muscle and mirabegron reducing urgency and frequency by increasing bladder storage capacity [7,10]. Moreover, preference for fixed-dose regimens of MRAs (n = 83, 75.5%) and β-3 agonists (n = 87, 79.1%) was primarily driven by their proven efficacy. The lower incidence of AEs was also crucial, mentioned by 69 (62.7%) and 80 (72.7%) urologists, respectively. This attention to tolerability is clinically significant, as low persistence still remains an important challenge in pharmacotherapy of LUTS [24,25]. The most frequently observed AEs with silodosin-mirabegron FDC, including dry mouth (n = 73, 66.4%), anejaculation (n = 69, 62.7%), headache (n = 67, 60.9%), and dizziness (n = 52, 47.3%), are consistent with known tolerability profiles of individual agents [10,26]. The high rate of anejaculation indicates uroselectivity of silodosin, as the incidence of ejaculatory dysfunction is significantly greater with silodosin than placebo [10].

Notwithstanding moderate adherence reported by 95 (86.4%) urologists (25%-75% adherence range), patient feedback mainly remained positive, with 51 (46.4%) reporting combined improvements in QoL and symptomatic improvement. This demonstrates that even partial adherence may result in clinically significant benefits. The moderate adherence rates, however, emphasize a continuing challenge; in real-world scenarios, persistence with BPH medications is 29% at one year, with even lower rates for combination therapy (9%) [11,25]. These findings suggest that efficacy by itself does not ensure the best possible compliance.

The most frequently observed LUTS pattern was a combination of storage, voiding, and post-micturition symptoms (n = 59, 53.6%), followed by a combination of storage and voiding symptoms (n = 26, 23.6%). Pure storage (n = 11, 10.0%) or voiding symptoms (n = 13, 11.8%) were seldom observed. This distribution highlights that multiple pathophysiologic mechanisms are often involved in LUTS in Indian men, which supports the justification for combination therapy that targets detrusor overactivity as well as bladder outlet obstruction [20].

However, certain findings deviate from prescribing practices observed in the Western world. Given that tadalafil for BPH is not always reimbursed in Indian healthcare settings, the comparatively lower preference for PDE5Is (n = 75, 68.2% frequent use) in comparison to European settings may be due to financial concerns [27]. Moreover, the restricted evidence base for LUTS indications is consistent with the limited use of SNRIs (n = 40, 36.4% less frequent, n = 41, 37.3% rarely used) [24].

Limitations

Due to the cross-sectional, questionnaire-based design, this survey has certain limitations. First, recall bias could have affected the responses, because urologists might underreport less preferred prescribing practices or overreport adherence to guidelines. Second, the sample size was small and mainly represented non-metropolitan practitioners (90%) with 5-15 years of experience, which may limit their applicability to more senior urologists or those practicing in metropolitan cities. Third, objective clinical parameters, including urodynamic results, prostate volume, and prostate-specific antigen levels, which have an impact on treatment choices, were not included in the survey. Fourth, the study relies entirely on physicians’ perceptions regarding AEs, adherence, and patient satisfaction, rather than objective patient-reported or clinical data. Fifth, the questionnaire was not formally validated or pilot-tested. Sixth, urologists were recruited through convenience sampling from professional networks and subsequent referrals, which may limit generalizability and introduce selection bias. Finally, the lack of assessment of patient-level outcomes, including actual adherence, persistence, and clinical response, represents a crucial area for further evaluation.

Conclusions

This nationwide survey shows that Indian urologists prefer α1-blockers, especially silodosin, as the first-line monotherapy for LUTS in men. Among the urologists surveyed, strong preference for the silodosin-mirabegron FDC indicates increasing clinical confidence in dual-mechanism strategies that treat storage and voiding symptoms. In clinical practice, dutasteride has largely supplanted finasteride. Patient-reported outcomes are generally favorable, but adherence is still moderate. These findings provide opportunities for focused educational interventions to improve LUTS management and offer useful real-world evidence to supplement clinical trial data.

Acknowledgments

The authors would like to thank Dr. Vikas S. Sharma (MD), CEO, Maverick Medicorum® (www.maverickmedicorum.com), for statistical analyses as well as manuscript writing, editing, submission, and post-submission services. The authors have no conflict of interest with Dr. Vikas S. Sharma or Maverick Medicorum® (India).

Appendices

Figure 1. Study questionnaire.

Figure 1

Disclosures

Human subjects: Informed consent for treatment and open access publication was obtained or waived by all participants in this study. Central Independent Ethics Committee, Pune, Maharashtra issued approval CIEC/2025/0408.

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:

Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.

Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.

Other relationships: Both Shubhra Dhurandhar and Dr. Sanjay Kamble are employees of Samarth Life Sciences Pvt Ltd. (Mumbai).

Author Contributions

Concept and design:  Sanjay Kamble, Prakash Patwardhan, Rahul Sharma, Shubhra Dhurandhar

Acquisition, analysis, or interpretation of data:  Sanjay Kamble, Prakash Patwardhan, Santosh Palkar, Rahul Sharma, Shubhra Dhurandhar

Drafting of the manuscript:  Sanjay Kamble, Prakash Patwardhan, Santosh Palkar, Rahul Sharma, Shubhra Dhurandhar

Critical review of the manuscript for important intellectual content:  Sanjay Kamble, Prakash Patwardhan, Santosh Palkar, Rahul Sharma, Shubhra Dhurandhar

Supervision:  Sanjay Kamble

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