Loading clinical trials...
Loading clinical trials...
Puncture to Repigment: A Comparative Analysis Of Needling vs. Microneedling Along With NBUVB in Treatment of Non-Segmental Vitiligo
This randomized controlled trial aims to compare the efficacy of needling versus microneedling, both followed by narrowband UVB therapy, in achieving repigmentation in patients with localized stable non-segmental vitiligo.
The study will enroll 80 patients aged 15-60 years with localized stable vitiligo. Participants will be randomized into two groups: one receiving needling and the other microneedling, each followed by NBUVB therapy. The primary outcome is the percentage of repigmentation at 12 weeks, assessed through digital planimetry and standardized clinical photography. Secondary outcomes include adverse effects such as erythema, post-inflammatory hyperpigmentation, infection, and scarring.
Age
15 - 60 years
Sex
ALL
Healthy Volunteers
No
Khyber Teaching Hospital
Peshawar, Khyber Pakhtunkhwa, Pakistan
Start Date
March 1, 2025
Primary Completion Date
August 31, 2025
Completion Date
August 31, 2025
Last Updated
September 2, 2025
80
ESTIMATED participants
Needling + NBUVB
PROCEDURE
Microneedling + NBUVB
PROCEDURE
Lead Sponsor
Khyber Teaching Hospital
NCT07431177
NCT07352293
NCT07437560
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions