Nanofat Grafting for Treatment of Androgenetic Alopecia

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Androgenetic alopecia
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Brief Title

Condensed Nanofat Grafting for Treatment of Androgenetic Alopecia

Official Title

Condensed Nanofat Grafting for Treatment of Androgenetic Alopecia

Brief Summary

      Nowadays, multiple treatment modalities have been applied clinically to treat androgenic
      alopecia, such as Follicular unit transplantation(FUT), finasteride, platelet-rich plasma
      injection(PRP), etc. In this clinical trial, the investigators aim to analyze the effect of
      nanofat grafting on treating androgenic alopecia in male.

Detailed Description

      The investigators will treat the hair loss area of a patient by processed nanofat grafting.
      The participants were asked to come back 1、3、6、9、12 months after treatment for further
      follow-up.

      Before and after the treatment, the hair and follicular will be assessed subjectively by
      satisfaction assessment, dermatoscope.

Study Type

Interventional

Primary Outcome

Dermatoscope

Condition

Androgenic Alopecia

Intervention

Nanofat grafting

Study Arms / Comparison Groups

 processed Nanofat grafting
Description:  processed autologous Nanofat will be injected into the area of the scalp with androgenic alopecia.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status

Procedure

Estimated Enrollment

10

Start Date

February 27, 2019

Completion Date

May 1, 2020

Primary Completion Date

February 27, 2020

Eligibility Criteria

        Inclusion Criteria:

          -  Male patients with androgenic alopecia aging from 18 to 50.

          -  No scars and wounds on the alopecia area.

          -  No skin disease or serious cardiovascular disease.

          -  Preoperative examinations remain healthy.

        Exclusion Criteria:

          -  Serious chronic heart, liver, kidney, blood system disease

          -  Allergic diseases, skin inflammation or wounds

          -  Alopecia but not androgenic alopecia

          -  Acute or chronic infection

          -  Take anticoagulant drugs

          -  Active vitiligo, psoriasis, systemic lupus erythematosus

Gender

Male

Ages

18 Years - 50 Years

Accepts Healthy Volunteers

Accepts Healthy Volunteers

Contacts

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Location Countries

China

Location Countries

China

Administrative Informations

NCT ID

NCT03506503

Organization ID

2019004

Responsible Party

Principal Investigator

Study Sponsor

Jinan University Guangzhou

Study Sponsor

, ,

Verification Date

February 2021