PACTR202607567738879Active, not recruitingPhase 3
Microneedling with methotrexate versus intralesional steroid in the treatment of localized vitiligo
Conditions
Interventions
Trial Snapshot
- Phase
- Phase 3
- Status
- Active, not recruiting
- Sponsor
- Al Azhar university
- Enrollment
- 36
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Year(s) to 44 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Co-operative patient who is willing and able to comply with the treatment protocol and follow-up visits.
- •Participants must have stable vitiligo, meaning that the extent and severity of their vitiligo have not significantly changed in the past 6 months
Exclusion Criteria
- •Patients with keloidal tendency.
- •Patients receiving topical or systemic treatment for vitiligo and phototherapy during the previous 6 months.
- •Patients with active lesions.
- •Participants with a history of hypersensitivity to methotrexate or any of its excipients.
- •Participants with a history of liver disease or liver function abnormalities.
- •Participants with a history of bleeding disorders or receiving anticoagulant therapy.
- •Participants who are pregnant or breastfeeding.
- •Participants with active skin infections or skin conditions that would contraindicate the use of microneedling or intralesional injections.
Arms & Interventions
;Intralesional steroids;Microneedling with methotrexate
Intervention: ;Intralesional steroids;Microneedling with methotrexate
Investigators
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