Actively Recruiting

Phase 1
Phase 2
Age: 25Years - 59Years
All Genders
NCT07429253

Secretome vs. PRP Injections for Hair Density and Growth in Androgenetic Alopecia Patients

Led by PT. Prodia Stem Cell Indonesia · Updated on 2026-02-24

40

Participants Needed

1

Research Sites

37 weeks

Total Duration

On this page

Sponsors

P

PT. Prodia Stem Cell Indonesia

Lead Sponsor

R

RS Prof. Dr. I.G.N.G Ngoerah

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to compare the effectiveness of secretome injection and intradermal platelet-rich plasma (PRP) injection on hair density and the terminal-to-vellus hair ratio in patients with androgenetic alopecia at Prof. Dr. I.G.N.G. Ngoerah General Hospital.

CONDITIONS

Official Title

Secretome vs. PRP Injections for Hair Density and Growth in Androgenetic Alopecia Patients

Who Can Participate

Age: 25Years - 59Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male patients aged 25 to 59 years with androgenetic alopecia, Hamilton-Norwood grades II to VI, seeking treatment at Prof. Dr. I.G.N.G. Ngoerah General Hospital
  • Female patients aged 25 to 59 years with androgenetic alopecia, Ludwig grades I to III, seeking treatment at the same hospital
  • Female patients not currently pregnant or breastfeeding
  • Patients who have stopped anti-androgen medication and minoxidil for at least 1 month before treatment
  • Patients without known allergies to secretome components or PRP preparation materials
  • Patients able to speak Indonesian and willing to give written informed consent
Not Eligible

You will not qualify if you...

  • Patients unable to speak or understand Indonesian or unwilling to provide written informed consent
  • Patients with hair loss types other than androgenetic alopecia
  • Patients currently using 5-alpha reductase inhibitors
  • Patients who had intradermal corticosteroid injections to the scalp within 6 months before the study
  • Patients with active scalp infections or dermatitis
  • Patients with known allergies to secretome components or PRP preparation materials
  • History of hypertrophic scarring or blood clotting disorders
  • Patients unable to complete all study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Prof. dr. I.G.N.G. Ngoerah Central General Hospital

Denpasar, Bali, Indonesia, 80113

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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