Clinical Study of PRP in the Treatment of Androgenetic Al... | NCT07551271

Studies
Clinical Study of PRP in the Treatment of Androgenetic Alopecia

NCT07551271

Sponsor

The First Affiliated Hospital of Soochow University

Status

Completed

Last Update Posted

Apr 24, 2026Actual

Enrollment

30Actual

Phase

Not Applicable

Conditions

Androgenetic Alopecia (AGA)

Interventions

Countries

China

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Apr 2026

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 1, 2025Actual

Primary Completion Date

Jan 1, 2026Actual

Completion Date

Mar 1, 2026Actual

First Submitted Date

Apr 19, 2026

First Submission Date that Met QC Criteria

Apr 19, 2026

First Posted Date

Apr 24, 2026Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Apr 19, 2026

Last Update Posted Date

Apr 24, 2026Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

A study on the therapeutic effect of platelet-rich plasma in the treatment of androgenetic alopecia

Detailed Description

This study included 30 patients with moderate and severe androgenic alopecia and randomly divided into two groups, group A was treated with platelet-rich plasma (once 4 weeks for 3 times) combined with external Minoxidil(5% for male, 2% for female, twice a day, 1 ml each time) , group B was treated with external Minoxidil. The patients in both groups were examined by dermoscopy before the first treatment and 1,2,3 and 6 months after the treatment. The scalp MRI was performed before the first treatment and 6 months after the treatment, the number, density and depth of hair follicles were measured to evaluate the efficacy and safety of platelet-rich plasma combined with Minoxidil in the treatment of androgenic alopecia.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

30Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
group A	Experimental	platelet-rich plasma combined with minoxidil	Drug: PRP

Interventions

Name	Type	Description	Arm Group Labels	Other Names
PRP	Drug	group A was treated with platelet-rich plasma combined with external Minoxidil , group B was treated with external Minoxidil	group A

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Dermoscope	The amount of hair on the parietal and posterior occipital regions	before the first treatment and 1,2,3 and 6 months after the treatment
MRI	Hair follicle density on the parietal and posterior occipital regions	before the first treatment and 6 months after the treatment

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

moderate to severe androgenic Alopecia

Exclusion Criteria:

abnormal coagulation

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

Not provided

Maximum Age

Not provided

Standard Ages

ChildAdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Not provided

Locations

Facility	Status	City	State	ZIP	Country	Contacts
the First Affiliated Hospital of Soochow University		Suzhou	Jiangsu	215300	China

IPD Sharing Statement Module

Plan to Share IPD

Undecided

Description

Not provided

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D000505	Alopecia

Ancestor Terms

ID	Term
D007039	Hypotrichosis
D006201	Hair Diseases
D012871	Skin Diseases
D017437	Skin and Connective Tissue Diseases

Browse Leaves

Not provided

Browse Branches

Not provided