Comparison Between Systemic Steroids, Topical Steroids, or Calcineurin Inhibitors With Mini Punch Grafting in Treatment of Stable Non-segmental Vitiligo
Vitiligo
About this trial
This is an interventional treatment trial for Vitiligo focused on measuring vitiligo, mini punch grafting, oral mini pulse steroids, topical treatment
Eligibility Criteria
Inclusion Criteria:
Patients of either gender aged more than 18 years old, with stable resistant non-segmental vitiligo will be included.
Stability is defined in terms of:
- Absence of new lesions or extension of preexisting lesions prior to presentation for the last 6 months.
- Absence of koebner phenomenon, confetti lesions or hypopigmented lesions, or lesions with ill-defined borders during this same time period.
Absence of activity signs by dermoscopic examination which includes :
- Ill-defined or trichrome border.
- Micro-Koebner's phenomenon.
- Tapioca sago appearance.
- Starburst appearance.
- Comet tail appearance.
- Altered pigment network. Resistance to treatment is defined in terms of not responding or those responding poorly to administered treatment (<25% repigmentation according to VASI score) over the last 3 months, especially in patients having lesions on glabrous skin or those with lesions showing leukotrichia.
Exclusion Criteria:
Cases of active, the progressive disease having any of the features of activity listed above during the last 6 months.
Patients with regressive disease showing evidence of repigmentation under administered therapy.
Patients with segmental vitiligo or vitiligo affecting more than 70% body surface area.
Patients with associated autoimmune diseases or any other comorbidity. Patients with a tendency towards hypertrophic scars or keloid formation. Pregnant and breast-feeding females. Patients with psychological instability and unrealistic expectations.
Sites / Locations
- Alexandria faculty of medicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
high dose oral steroids
low dose oral steroids
topical treatment
(20 patients) will receive high dose oral mini pulse steroids (dexamethasone 5 mg on two consecutive weekly days for 3 months).
(20 patients) will receive low dose oral mini pulse steroids (2.5mg dexamethasone on two consecutive weekly days for 3 months
(20 patients) chosen lesions of comparable size and location in each patient in this group will receive either; super potent topical steroids once every other day, Tacrolimus ointment twice daily for 3 months, or nothing to serve as a control.