Vitiligo. Vitiligo
Conditions
Interventions
Comparable vitiliginous lesions were selected from both sides of the body. On Day 0, heavily pigmented follicular grafts were harvested from the scalp by follicular unit extraction and transplanted in
Dr. Honle medizinitechnik, GmbH, Germany) three times a week until Day 60±4
phototherapy was restarted on day 71±2. The phototherapeutic dose was increased by 15% at each treatment interval and was completed by Day 100±4 (for a total of 12 weeks of treatment). Clobetasol 45%
Treatment - Surgery
phototherapy was restarted on day 71±2. The phototherapeutic dose was in
Sponsors
Vice chancellor for research, Jahrom University of Medical Sciences
Eligibility
Sex/Gender
All
Age
12 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria included:All patients were dermatologically diagnosed with refractory, palmar-plantar vitiligo exclusion criteria included:hypersensitivity to laser and hair transplantation materials
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Scale of pigmentation improvement of lesion( scale of repigmentation). Timepoint: in Three month ,each month once after intervention. Method of measurement: The scale of repigmentation (increase the amount of pigment in vitiligo patches) will be classified based on percentage of improvement in 4 grades. The ratings are: Scale 0: no repigmentation- Scale 1: Returning pigmentation between 0% to 25% which is mild pigmentation- Scale 2: The return of pigmentation 25% and 50% which is average- Scale 3: Good pigmentation which is between 50% to 75%- Scale 4: the return of pigmentation between 75% and 100% which is considered excellent. Measurements are performed by a physician through examination under a Wood's lamp and photography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Complications due to interventions. Timepoint: 1 week, 4 week, 2 months, 4 months and 6 months after start of treatment. Method of measurement: Every kind of local or generalized complication due to intervention which according to the confirm of dermatologist should be recorded in the questionnaire. These complications are usually redness and irritation at the site of intervention. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNavid Kalani
Jahrom University of Medical Sciences
Outcome results
None listed