The Effect of Platelet-rich Plasma in Subjects With Androgenetic Alopecia

NCT ID: NCT03048461

Last Updated: 2021-12-23

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-06-30
• Study Completion Date: 2020-12-31

Brief Summary

The purpose of this study is to evaluate the effect of autologous platelet-rich plasma (PRP) in the treatment of androgenetic alopecia.

This is a randomized clinical trial to evaluate the effect of autologous platelet rich plasma in subjects with moderate androgenetic alopecia. Approximately 30 subjects will be randomized into the study. The study is designed as an 18-month study consisting of 2 phases. This study was a pilot study designed to determine feasibility of this procedure.

Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be considered for enrollment.

Conditions

Androgenetic Alopecia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Platelet Rich Plasma

Participants will receive intradermal injections autologous PRP to an area (100cm2) of alopecia on the scalp.Two treatments will be performed 3 months apart

Group Type: EXPERIMENTAL

Platelet Rich Plasma Prep System

Intervention Type: DEVICE

intradermal injections of platelet rich plasma to an area of alopecia

Placebo (sterile saline)

Participants will receive intradermal injections of sterile normal saline to an area (100cm2) of alopecia on the scalp. Two treatments will be performed 3 months apart

Group Type: PLACEBO_COMPARATOR

Platelet Rich Plasma Prep System

Intervention Type: DEVICE

intradermal injections of platelet rich plasma to an area of alopecia

Placebo

Intervention Type: DRUG

intradermal injections to an area of alopecia

Interventions

Platelet Rich Plasma Prep System

intradermal injections of platelet rich plasma to an area of alopecia

Intervention Type: DEVICE

Placebo

intradermal injections to an area of alopecia

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Males or females ≥ 18 years old and ≤55 years old

2. Subjects are in good health as judged by the investigator.

3. Diagnosed with by a dermatologist with moderate androgenetic alopecia.

4. Subject is seeking treatment for androgenetic alopecia.

5. Subject has never previously used finasteride or minoxidil or has consistently used finasteride or minoxidil for at least 1 year.

6. Subjects who are willing and have the ability to understand and provide informed consent for participation in the study and are able to communicate with the investigator.

Exclusion Criteria

1. Other than androgenetic alopecia, evidence of another skin condition affecting the treatment area that would interfere with clinical assessments.

2. Subjects who are unwilling to avoid initiating treatment with minoxidil or finasteride for the duration of the study; or in subjects who have been treated with minoxidil or finasteride for at least 1 year, unwilling to avoid changes in the dosing regimen of these medications for the duration of the study.

3. Willing to refrain from washing hair or using hair product 24 hours before and after treatment visits

4. History of a clinically significant hematologic disorder as determined by the investigator.

5. Subjects currently receiving anticoagulant or anti-platelet therapy.

6. Subjects on daily Aspirin therapy for cardiovascular disease.

7. Subjects with chronic NSAID use, unable to wean off.

8. Subject is known to be HIV positive.

9. History of recurrent facial or labial herpes simplex infection

10. History of hypertrophic scars or keloids

11. Known genetic disorders affecting fibroblasts or collagen, such as achondroplasia, osteogenesis imperfecta, etc.

12. Subjects who have any requirement for the use of local or systemic steroids or other immunosuppressive agent

13. Pregnant or breast feeding

14. Uncooperative patients or patients with neurological disorders who are incapable of following directions or who are predictably unwilling to return for follow-up examinations.

15. Subjects who are unable to understand the protocol or give informed consent.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Northwestern University

OTHER

Sponsor Role: lead

Responsible Party

Murad Alam

MD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Murad Alam, MD

Role: PRINCIPAL_INVESTIGATOR

Northwestern University

Countries

United States

Other Identifiers

MA04222016

Identifier Type: -

Identifier Source: org_study_id