Efficacy and Safety Of Oral Minoxidil in the Treatment of Male Androgenetic Alopecia in a Tertiary Care Center
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 55
- 试验地点
- 1
- 主要终点
- Improvement in the parameters of the hair analysis namely the increase in the number of hairs per cm2 and increase in the hair diameter measured by Foto finder and an improvement in photographic assessment done by two independent observers
研究概览
简要总结
Androgenetic Alopecia is the most common type of non-scarring alopecia in male. The aim of the study is to evaluate the efficacy and safety profile of low dose oral minoxidil (2.5mg) in male suffering from androgenetic alopecia. The study is planned for 12 months. The subjects will be selected and observed from among the patients who come for the treatment of MAGA, who are not on any treatment for the past 3 months, has undergone trichoscan examination and has been started on 2.5 mg of oral minoxidil for the treatment of the same. Socio-demographic data, global photographic assessment and trichoscan findings will be collected using a proforma after obtaining consent.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- Male
入选标准
- •Patients diagnosed with Male Androgenetic Alopecia with typical clinical presentation and trichoscopic finding. Patients between the age of 18.
排除标准
- •Those who are not willing for the study and who has been on treatment for hair loss for the past 3 months.
- •Patient with cardiac disease and hypotension.
结局指标
主要结局
Improvement in the parameters of the hair analysis namely the increase in the number of hairs per cm2 and increase in the hair diameter measured by Foto finder and an improvement in photographic assessment done by two independent observers
时间窗: 4 months
次要结局
- Improvement in the patient satisfaction score analyzed by the questionnaire(4 months)
研究者
Dr Farha P Nazeer
Medical Trust Hospital