CTRI/2023/11/059621尚未招募2 期
An open label, non randomized, interventional study to evaluate the efficacy and safety of microneedling combined with 5-fluorouracil 5% cream versus microneedling combined with tacrolimus 0.1% ointment versus microneedling alone in clinically stable vitiligo patients - NI
Dr Sushnitha Johnson0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.All patients aged from 18 to 50 years with localized & stable vitiligo for a year willing to come for regular follow up. 2.No history of topical application for 2 weeks, oral medication for 4 weeks, phototherapy and excimer laser for 8 weeks when enrolled in the study. 3.Patients with 3 or more stable vitiligo patches
排除标准
- •1.Pregnant or lactating women
- •2.Presence of Bleeding /coagulation disorders
- •3.Past history of keloidal tendency
- •4.Patients with active infections
- •5.Patients with known allergy to 5-fluorouracil, tacrolimus
- •6.Immunosuppressed patients
- •7.Any concomitant skin conditions over the vitiligo patch
- •8.Mucosal and palmoplantar vitiligo
研究者
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