Table 1.
Source | Study Design | Types of Vitiligo |
No. of Patients |
Subtype | Treatment Duration | Intervention | Fitzpatrick Skin Type | Types of Topical Vit-D |
Outcome |
---|---|---|---|---|---|---|---|---|---|
Abdel 2015 [78] | Randomized blinded comparative study | Non-segmental | 44 | Localized and stable | 3 months |
|
NR | Ointment |
|
Ada 2005 [79] | Right-left comparison prospective single-blinded study | Non-segmental | 20 | Generalized vitiligo | 12 months |
|
NR | Cream |
|
Akdeniz [80] 2014 | Randomized double-blind comparative study | Non-segmental | 45 | NR | 6 months |
|
NR | Ointment |
|
Arca 2006 [81] | Comparative prospective study | Non-segmental | 40 | Stable | 4 months |
|
NR | Ointment |
|
Bakr 2021 [82] | Prospective randomized comparative study | Non-segmental | 30 | Stable | 3 months |
|
NR | Ointment |
|
Baysal 2003 [47] | Prospective right/left comparative, open study | Non-segmental | 22 | Generalized | 9 months |
|
NR | Cream |
|
Cherif 2003 [83] | Prospective study | Non-segmental | 23 | Bilateral symmetrical | 15 weeks |
|
IV, V | Ointment |
|
Gargoom 2004 [84] | Prospective right/left comparison study | Segmental and non-segmental | 18 | Focal/mucosal | 4–6 months |
|
NR | Cream/Ointment |
|
Goktas 2006 [75] | Prospective right/left comparison study | Non-segmental | 24 | Generalized | 6 months |
|
II, III | Cream |
|
Goldinger 2007 [85] | Prospective right/left comparative single-blinded trial | Non-segmental | 10 | Bilateral symmetrical | 15 months |
|
II, III, IV | Ointment |
|
Hartmann 2005 [86] | Prospective right/left comparative study | Non-segmental | 10 | Symmetrical (vulgaris/acrofacial /localized) | 12 months |
|
II, III | Ointment |
|
Ibrahim 2019 [87] | Prospective right/left comparative study | Segmental and non-segmental | 25 | Stable and symmetrical, focal and generalized | 6 months |
|
III, IV | Ointment | 60% showed excellent improvement for the calcipotriol combination compared to 32% for tacrolimus |
Juntongjin 2021 [88] | Prospective randomized double-blind comparative study | Non-segmental | 13 | Acral vitiligo | 24 weeks |
|
IV | Ointment |
|
Katayama 2003 [89] | Prospective uncontrolled open trial | Segmental and non-segmental | 15 | Vulgaris vitiligo | 3 months |
|
NR | Ointment | 40% of patients responded in a good to excellent way clinically |
Khullar 2015 [90] | Prospective right-left comparative study | Non-segmental | 27 | Generalized vitiligo (vulgaris and acrofacial | 24 weeks |
|
III, IV, V | Ointment | 51.4% reduction in the lesions for NB and 49% for combination (good repigmentation) |
Kullavanija-ya 2004 [91] | Prospective open bilateral comparison study | Non-segmental | 20 | Symmetrical vitiligo | 15 months |
|
NR | Ointment |
|
Kumaran 2006 [92] | Randomized trial | Non-segmental | 49 | Localized vitiligo | 3 months |
|
NR | Ointment |
|
Leone 2006 [93] | Prospective randomized open-label study | Non-segmental | 32 | Generalized and symmetrical | 12 months |
|
II, III, IV | Ointment |
|
Lotti 2008 [94] | Prospective open study | Segmental and non-segmental | 470 | Vulgaris vitiligo | 6 months |
|
I, II, III, IV | Ointment |
|
Lu-Yan 2006 [95] | Randomized single-blind within a patient-controlled trial | Segmental and non-segmental | 38 | Symmetrical, localized, vulgaris | 8 weeks |
|
NR | Cream | 25.7% excellent repigmentation in the combination (early pigmentation with lower total dosage) to 5.7% for excimer monotherapy |
Oh 2011 [96] | Prospective randomized single-blinded paired comparative study | Non-segmental | 20 | Localized | 16 weeks |
|
NR | Ointment |
|
Onita 2004 [97] | Prospective open trial | Segmental and non-segmental | 27 | Vulgaris vitiligo | NR |
|
NR | Ointment | 48% of patients improved > 30%(moderate) |
Rodriguez 2009 [98] | Randomized double-blind placebo-controlled study | Non-segmental | 80 | NR | 4 months |
|
NR | Ointment | There was no reduction of the size of the lesion < 25% (poor repigmentation) |
Sahu 2016 [99] | Prospective open label right/left intraindividual trial | Non-segmental | 30 | Symmetrical vitiligo | 24 weeks |
|
NR | Ointment | 16.6% had moderate. 53.3% good 30% excellent repigmentation at the end of therapy |
Salem 2023 [100] | Prospective comparative study | Segmental and non-segmental | 25 | Stable vitiligo | 19 months |
|
II, III, IV | Solution | 52% excellent to good response in the combination |
Vazquez 2003 [101] | Prospective open pilot study | Non-segmental | 10 | NR | NR |
|
NR | Ointment |
|
Xing 2012 [102] | Prospective open uncontrolled trial | Segmental and non-segmental | 31 | Focal or generalized | 12 weeks |
|
NR | Ointment |
|
Abbreviations: NR, Not Reported; PUVA, Psoralens Long Wave Ultraviolet Radiation; NB-UVB, Narrowband Ultraviolet Phototherapy; MEL, Monochromatic excimer light; BM, Betamethasone.