Comparison Between Platelet Rich Plasma and Nanofat as an Adjuvant Therapy in HairTransplantation

December 3, 2025 updated by: Shenoda Gamel Fayez, Sohag University

Comparison Between Platelet Rich Plasma and Nanofat as an Adjuvant Therapy in Hair Transplantation in Male Androgenic Alopecia

  • To compare the efficacy of platlet rich plasma and Nanofat injection as adjuvant therapies with FUE hair transplantation in improving graft survival rate,
  • To measure hair density and thickness postoperatively using dermoscopy or trichoscopy.
  • To evaluate patient satisfaction and photographic assessment by blinded evaluators.
  • To assess any adverse effects or complications related to each modality

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

  • Ideal candidates for hair transplantation typically present with a clear, stable pattern of hair loss, characterized by at least 50% thinning or balding in 1 or more areas. The scalp must be healthy, with donor hair of good quality and quantity. Patients must have realistic expectations and be free of medical conditions that compromise surgical outcomes. The safe donor zone is located in the mid-occipital region between the upper and lower occipital protuberances, typically containing 65 to 85 follicular units/cm²
  • Intra-operative injection of PRP is beneficial in giving faster density, reducing the catagen loss of transplanted hair, early recovery of the skin, the faster appearance of new anagen hair in FUE hair transplantation.
  • This study compares the effects of PRP and Nano fat as adjuvants in Androgenic alopecia patients undergoing FUE hair transplantation.
  • Nanofat contain stem cells supposed to improve the results of FUE hair transplantation , but the question that we hope to answer at the end of our study which one we recommend as an adjuvant therapy PRP or Nano fat?

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • 1. Male patients with stable androgenic alopecia more than 2 years. 2. Age 20-50 years 3. No recent medical hair loss treatments.

Exclusion Criteria:

  • 1. Active scalp infections or scarring alopecia. 2. Systemic diseases affecting wound healing. 3. Platelet disorders or anticoagulant use. 4. Smoking or heavy alcohol intake

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: group a
hair transplantation done alone without platelet rich plasma or nanofat injection
we compare the effect of nanofat injection and platelet rich plasma in hair transplantation in male androgenic alopecia
Other Names:
  • hair transplantation with platelet rich plasma
  • hair transplantation with nanofat injection
Experimental: group b
we do injection of platelet rich plasma with hair transplantation
we compare the effect of nanofat injection and platelet rich plasma in hair transplantation in male androgenic alopecia
Other Names:
  • hair transplantation with platelet rich plasma
  • hair transplantation with nanofat injection
Experimental: group c
we do injection of nanofat with hair transplantation
we compare the effect of nanofat injection and platelet rich plasma in hair transplantation in male androgenic alopecia
Other Names:
  • hair transplantation with platelet rich plasma
  • hair transplantation with nanofat injection

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
• To measure hair density using dermoscopy.
Time Frame: • All patients will be followed up about 6-12 months postoperative.
To measure how many hair follicles in each cubic centimetre
• All patients will be followed up about 6-12 months postoperative.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: samia saied, MD, Sohag University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 1, 2026

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

November 22, 2025

First Submitted That Met QC Criteria

December 3, 2025

First Posted (Actual)

December 17, 2025

Study Record Updates

Last Update Posted (Actual)

December 17, 2025

Last Update Submitted That Met QC Criteria

December 3, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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