跳至主要内容
临床试验/NCT02591355
NCT02591355已完成不适用

A Monocentric, Double-blind, Randomized, Active- and Placebo-controlled Split-scalp Study to Evaluate the Clinical Effectiveness of Platelet-rich Plasma (PRP) in the Treatment of Androgenetic Alopecia

Regen Lab SA3 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2017年9月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Regen Lab SA
入组人数
80
试验地点
3
主要终点
Evaluate the changes in hair density of androgenetic alopecia

研究概览

简要总结

Platelet rich plasma (PRP) therapy is a novel therapeutic modality that has seen broad applications for a number of medical indications including those in orthopedics, dentistry, and dermatology. In dermatology, its uses have included treatment of chronic wounds and facial rejuvenation. More recently, anecdotal reports have suggested some efficacy in the treatment of hair loss, but to the best of our knowledge, there has been only one published case series documenting its use for this indication.

详细描述

This study was designed to better assess the efficacy of PRP in hair loss, we therefore propose to study interval intralesional PRP injections for patients with androgenetic alopecia (AGA). Androgenetic alopecia is the most common form of hair loss world-wide. Although there are currently numerous treatment options for this indication including minoxidil, 5-alpha reductase inhibitors and follicular unit transplant, many of the medical treatment options have undesirable side effects, particularly in women of child bearing age. These well-documented adverse reactions include impotency, hypertrichosis, and birth defects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women, age 18-60 with AGA
  • Completed informed consent form
  • Ludwig stage 1-2 for women
  • Norwood Hamilton Stage 3 to 5 for men

排除标准

  • Pregnancy or breastfeeding
  • Younger than 18 years
  • Uses of minoxidil and/or 5-alpha reductase inhibitors (such as finasteride or dutasteride) within 3 months of enrolling in the study
  • History of hair transplantation
  • Use of any cosmetic product aimed at improving or correcting the signs of hair loss within 2 weeks prior to screening
  • Facial cancer (squamous and basal cell carcinoma, melanoma)
  • Hereditary or acquired hematologic/coagulation disorders such as: platelet dysfunction syndrome, critical thrombocytopenia, hypofibrinogenemia, impaired coagulation, drepanocytosis (sickle cell anemia).
  • Hemodynamic instability
  • Acute infection
  • Auto-immune disease such as Hashimoto, rheumatoid arthritis, or lupus (exception: vitiligo and alopecia areata)
  • Malignancy with or without metastatic disease
  • Chemotherapy
  • Dermatological diseases affecting the face (e.g. porphyria)
  • Anticoagulant therapy
  • Patients taking Aspirin or other NSAIDs (Nonsteroidal anti-inflammatory drugs) such as Nurofen, Voltaren, Diclofenac or Naproxen can participate, provided medication is interrupted 7 days before beginning of the treatment
  • Patients taking vitamin E supplements can participate, provided medication is interrupted 14 days before beginning of the treatment

结局指标

主要结局

Evaluate the changes in hair density of androgenetic alopecia

时间窗: 5 months

Evaluate split scalp changes in hair density of androgenetic alopecia after 5 month treatment of Autologous Platelet Rich Plasma prepared with the RegenBCT-1 kit compared to other half of the scalp treated with saline solution.

次要结局

  • Evaluate the changes of hair diameter and hair shedding in androgenetic alopecia(5 months)

研究者

发起方
Regen Lab SA
申办方类型
Industry
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验