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临床试验/CTRI/2023/05/052909
CTRI/2023/05/052909尚未招募Unknown

A randomised three-armed comparative trial to study the efficacy of low dose oral minoxidil 2.5mg once daily versus 5% topical minoxidil twice daily versus 5% topical minoxidil twice daily +PRP combination in patients with androgenetic alopecia

Self1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年5月30日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
Self
入组人数
60
试验地点
1
主要终点
Proportion of patients showing improvement in modified Norwood-Hamilton scale by 1 grade in each group at end of 24 weeks

研究概览

简要总结

A randomised comparitive three-armed trial to study the efficacy of low dose oral minoxidil 2.5mg once daily versus 5% topical minoxidil twice daily versus 5% topical minoxidil twice daily and PRP combination in androgenetic alopecia. Patient followed up for 6 months, where improvement assessed using clinical photographs and videodermoscope. 5 patients of each group will be randomly selected for biopsy to study the nature of Treg cells and its signalling pathways post treatment.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 45.00 Year(s)(—)
性别
Male

入选标准

  • All androgenetic alopecia patients from Norwood Hamilton grade 3-5 are recruited.

排除标准

  • Patients suffering from other hair disorders, hypotensive episodes, irritant dermatitis to minoxidil, keloidal tendency and bleeding disorders.

结局指标

主要结局

Proportion of patients showing improvement in modified Norwood-Hamilton scale by 1 grade in each group at end of 24 weeks

时间窗: assessed at baseline, 4th month, 6th month

次要结局

  • Videodermoscopic assessment as proportion of patients showing 25% increase in hair density 25% decrease in hair diameter diversity and 25% decrease in number of vellus hair/mm2 by end of 24 weeks. Change in population of natural (CD25 high) and induced (CD25 low) T reg cells using Fluorescent activated cell sorting change in NOTCH pathway jagged 1 SOX 9 expression in hair follicle using immunofluorescence pre and post treatment(assessment done at baseline, 16 weeks and 24 weeks)

研究者

发起方
Self
申办方类型
Other [self]

研究点 (1)

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