Skip to main content
. 2023 Mar 3;120(9):146–154. doi: 10.3238/arztebl.m2022.0411

eTable 2. Evidence for treatment with intranasal topical corticoids in sinunasal olfactory dysfunction caused by chronic rhinosinusitis with polyposis (RCT).

Author Study participants Clinical endpoint Results
Xu et al.,
2020 (e92)
n = 127
1) Methylprednisolone 24 mg + budesonide NS for 1 week
2) Budesonide nasal drops + budesonide NS for 1 week
3) Budesonide NS for 1 week
VAS (0–10) Significant VAS improvement in all groups compared with baseline
No difference between the groups
Zeng et al.,
2019 (e93)
n = 187*
1) Fluticasone propionate NS for 3 months
2) Clarithromycin 250 mg for 3 months
VAS (0–10) Significant VAS improvement in both groups compared with baseline
No difference between the groups
Khan et al.,
2019 (e94)
n = 310
1) Mometasone furoate NS 1/d
2) Mometasone furoate NS 2/d
3) Placebo
Subjective assessment (0–3) Significant improvement compared with baseline only for 2 × daily nasal spray
Zhou et al.,
2016 (e95)
n = 748
1) Mometasone furoate NS 2/d
for 16 weeks
2) Placebo mometasone furoate
Subjective assessment (0–3) Significant improvement compared with placebo
Bangwala et al.,
2014 (e64)
n = 419
Review: 28 RCT
Meta-analysis: 5 RCT
Subjective assessment (0–3)
Objective testing
Significant improvement of olfaction by oral and topical steroids (improvement in 70% of the topical studies)
Jankowski et al.,
2009 (e96)
n = 246
1) Fluticasone propionate NS 2/d for 8 months
2) Fluticasone propionate NS 2/d for 1 month, Fluticasone propionate NS 1/d + placebo NS
for 7 months
3) Placebo NS for 2 months, then fluticasone propionate NS 2/d for 6 months
VAS (0–100)
Mean sense of smell disorder score
Significant improvement of both scores in corticoid groups compared with placebo
Ehnhage et al.,
2009 (e97)
n = 68
1) Fluticasone propionate nasal drops for 10 weeks
2) Placebo for 10 weeks
Subjective assessment (0–3)
Butanol threshold test
No significant improvement compared with placebo
Small et al.,
2008 (e98)
n = 447
1) Mometasone furoate NS for 4 months
2) Placebo
Subjective assessment (0–3) Significant improvement compared with placebo

*Also included patients who had chronic rhinosinusitis without polyposis

NS, Nasal spray; RCT, randomized controlled trial; VAS, visual analog scale