CTRI/2022/11/047692尚未招募4 期
Comparison of therapeutic efficacy and safety of two concentrations of intra-lesional triamcinolone acetonide in patchy alopecia areata of the scalp: an open label randomized trial
I0 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
- 4 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.Patients of both sexes(males and females), aged >13 years with AA,
- •2.Patients having AA on the scalp with <50% involvement.
- •3.Patients who had not taken any form of treatment in the last 8 weeks.
- •4.Patients who are willing to sign the written consent form before participating in the study
排除标准
- •1.Patients aged <13 years
- •2.Patients with alopecia totalis, alopecia universalis and ophiasis.
- •3.Patients having skin diseases affecting the scalp.
- •4.Patients with active infection at the local site and with keloidal tendency.
- •5.Pregnant or lactating women or immuno-compromised patients or patients with bleeding or coagulation disorders
研究者
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