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临床试验/CTRI/2024/09/073394
CTRI/2024/09/073394尚未招募1 期

Efficacy of autologous Growth Factor Concentrate injection and Platelet Rich Plasma injection in patients of Androgenic Alopecia receiving topical minoxidil: A randomized control trial

Shini Choubey1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年9月22日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
44
试验地点
1
主要终点
To compare the efficacy by comparing the final terminal and vellus hair ratio of both the groups.

研究概览

简要总结

Androgenic alopecia (AGA), is a common form of hair loss worldwide affecting both men and women, leading to significant psychosocial impacts. Topical minoxidil and oral finasteride are the only FDA-approved drugs for the treatment. With limited available drugs and their reported side effects, newer treatment modalities such as Platelet rich plasma (PRP), growth factor concentrate (GFC) and threads are being tried. This study aims to evaluate and compare the efficacy of GFC and PRP injections as an adjunct therapy to topical minoxidil in AGA patients.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • AGA patient: Hamilton and Norwood classification grade: II– IV in male and Ludwig classification grade – I and II female
  • Both male and female between 21-45 years of age.
  • Androgenic Alopecia patients who have not received any other systemic or topical treatment.

排除标准

  • Exclusion criteria:
  • Pregnant or lactating females
  • Patients with history of any existing scalp skin diseases (seborrheic dermatitis and scalp psoriasis), infections
  • Severe systemic illness (as uncontrolled DM or hypertension, liver or renal diseases)
  • Immunocompromised patients
  • Alopecia caused by other factors such as telogen effluvium, alopecia areata, or scarring alopecia.
  • Patients who are positive for HIV/ HBsAg /HCV/ VDRL.

结局指标

主要结局

To compare the efficacy by comparing the final terminal and vellus hair ratio of both the groups.

时间窗: Baseline and 3rd month.

次要结局

  • PATIENT SATISFACTION SCORE(PAIN GRADATION)

研究者

发起方
Shini Choubey
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Shini Choubey

Kalinga Institute of Medical Sciences

研究点 (1)

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