跳至主要内容
临床试验/CTRI/2024/04/065133
CTRI/2024/04/065133尚未招募Unknown

Comparative study for the efficacy of microneedling alone and microneedling with platelet rich plasma in male-pattern hairloss

Government Medical College and Hospital, Chandigarh1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年4月15日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
To evaluate the improvement in hair growth

研究概览

简要总结

A randomized comparative study is being conducted to evaluate the efficacy of microneedling alone vs microneedling with platelet rich plasma in the treatment of male pattern hairloss. Males above the age of 18 years diagnosed with AGA Hamilton grade 3, 4, 5 will be recruited and and randomly alllocated into two groups of 20 each. Only microneedling group will receive three sessions of microneedling at 0, 4 and 8 weeks. Microneedling with PRP group will receive three sessions of microneedling with PRP application at 0, 4 and 8 weeks. The efficacy and safety outcome measures will be the change in total and terminal hair count, scoring of the global photographs by evaluators, patient self assesment and adverse events, assessed in both the groups at baseline and at 4 weekly intervals at 4, 8 and 12 weeks.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
Male

入选标准

  • Males above the age of 18 years diagnosed with AGA Hamilton grade 3, 4, 5
  • New cases of male pattern hair loss
  • Previously treated cases not under any treatment for past 6 months.

排除标准

  • Malignancy or chemotherapy
  • Hematological or autoimmune disorder
  • Thrombocyte dysfunction, bleeding disorders or on anticoagulant therapy
  • Scalp area to be treated having any infection or dermatitis.

结局指标

主要结局

To evaluate the improvement in hair growth

时间窗: The three primary efficacy measures will be the change in total and | terminal hair count, scoring of the global photographs by evaluators and patient self assessment, | assessed in both the groups at baseline and at 4 weekly intervals at 4, 8 and 12 weeks.

次要结局

  • Adverse Effects of Treatment(At each follow up visits- 4, 8 & 12 weeks.)

研究者

发起方
Government Medical College and Hospital, Chandigarh
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Divya Aneela K

Government Medical College and Hospital, Chandigarh

研究点 (1)

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