Comparing platelet-rich fibrin and plasma for treating female pattern hair loss
A Randomized, Split-head Comparison Study of the Efficacy and Safety of Platelet-rich Fibrin and Platelet Rich Plasma in Female Pattern Hair Loss Patients : A Pilot Study
NA · Siriraj Hospital · NCT06440655
This study is testing whether platelet-rich fibrin or platelet-rich plasma is better and safer for treating women with female pattern hair loss.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 10 (estimated) |
| Ages | 20 Years to 55 Years |
| Sex | Female |
| Sponsor | Siriraj Hospital (other) |
| Locations | 2 sites (Bangkok Noi, Bangkok and 1 other locations) |
| Trial ID | NCT06440655 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the efficacy and safety of two treatments, platelet-rich fibrin and platelet-rich plasma, in women experiencing female pattern hair loss. Participants will receive three treatments of either intervention at one-month intervals, followed by follow-up assessments at four and six months post-treatment. The study will help determine which treatment is more effective and safer for this condition.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 20-55 diagnosed with female pattern hair loss classified as Ludwig Type 2.
Not a fit: Patients who are pregnant, lactating, or have certain medical conditions such as platelet dysfunction or active smoking may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective treatment option for women suffering from hair loss.
How similar studies have performed: Previous studies have shown promising results with platelet-rich plasma in hair restoration, but the comparison with platelet-rich fibrin is less explored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 20-55 years * Female * Subject who was diagnosed with Female pattern hair loss in Ludwig Classification 2 (part width 2-4 centimeters) by Dermatologist Exclusion Criteria: * Pregnancy or Lactation subjects * Subject with history of platelet dysfunction, low platelet, anemia, cirrhosis, cancer, or immunocompromised host * Subject who are active smoking and alcoholism * Subject who has dermatitis, scar or infection at intervention area * Subject who has history of allergy to anesthesia drug * Subject who taking NSAIDs, Hormonal drug, anticoagulants drug * Subject who has psychiatric condition diagnosed by psychiatrist * Subject who are not allowed to take a photo
Where this trial is running
Bangkok Noi, Bangkok and 1 other locations
- Faculty of Medicine Siriraj Hospital, Mahidol University — Bangkok Noi, Bangkok, Thailand (RECRUITING)
- Medicine Siriraj Hospital, Mahidol University — Bangkok Noi, Bangkok, Thailand (RECRUITING)
Study contacts
- Principal investigator: Rattapon Thuangtong, Asst. Prof. — Mahidol University
- Study coordinator: Rattapon Thuangtong, Asst. Prof.
- Email: rattaponthuangtong@yahoo.com
- Phone: +66815533305
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Female Pattern Hair Loss, Platelet-Rich Plasma, Platelet-rich Fibrin, female pattern hair loss, platelet-rich plasma, platelet-rich fibrin