Evaluating the Efficacy of Platelet-rich Plasma Therapy in the Treatment of Androgenic Alopecia

NCT ID: NCT03474718

Last Updated: 2025-11-21

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-04-30
• Study Completion Date: 2027-06-30

Brief Summary

The study team will assess the efficacy of platelet-rich plasma therapy, a special blood product which is from the participant's own body, in the treatment of androgenic alopecia (also known as male pattern hair loss) in females.

Detailed Description

Androgenic alopecia, or male-pattern hair loss affects both men and women. This hair loss pattern is typically characterized by thinning at the crown of scalp and/or M-shaped hair line in males or diffuse thinning throughout in females. Platelet-rich plasma (PRP) therapy has recently been studied as a hair rejuvenation therapy in patients with non-inflammatory alopecia. Though the mechanism of action is not well understood, PRP is thought to promote angiogenesis and enhance blood flow around hair follicles via platelet-derived growth factor (PDGF), transforming growth factor (TGF), and vascular endothelial growth factor (VEGF). The primary objective of the study is to determine whether PRP, administered once monthly for 3 months improves clinical outcomes and quality of life in females with androgenic alopecia. This is a randomized, placebo-controlled, double-blind, half-head, single center clinical study where sixteen subjects with androgenic alopecia will be recruited. Dermatology Life Quality Index will be assessed at several time points. Disease severity will be measured using the Severity of Alopecia Tool (SALT), Alopecia Density and Extent Score (ALODEX); Trichoscan images will be captured to document participants' clinical progress. Adverse events will be recorded at each visit, treatment will be discontinued if any subject experience a serious adverse event. Treatment visits will take place at baseline, 4 weeks (1 month), 8 weeks (2 months), and 12 weeks (3 month). A follow-up, non-treatment visit will take place at 24 weeks (6 months). The study team hypothesizes that PRP will improve DLQI, SALT, ALODEX, hair count (number of hairs/0.65 cm2), hair density (number of hairs/cm2), hair diameter, anagen to telogen ratio, and vellus hair to terminal hair ratio in female subjects with androgenic alopecia.

Conditions

Androgenic Alopecia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Group A

At the baseline visit subjects will be randomized to either group A or group B. Group A will receive PRP on left side of scalp and placebo (saline solution) on right side of scalp.

Group Type: EXPERIMENTAL

Platelet-rich Plasma Left Side

Intervention Type: BIOLOGICAL

Group A will receive PRP on left side of scalp and placebo (saline solution) on right side of scalp.

Group B

At the baseline visit subjects will be randomized to either group A or group B. Group B will receive PRP on right side of scalp and placebo (saline solution) on left side of scalp.

Group Type: EXPERIMENTAL

Platelet-rich Plasma Right Side

Intervention Type: BIOLOGICAL

Group B will receive PRP on right side of scalp and placebo (saline solution) on left side of scalp.

Interventions

Platelet-rich Plasma Left Side

Group A will receive PRP on left side of scalp and placebo (saline solution) on right side of scalp.

Intervention Type: BIOLOGICAL

Platelet-rich Plasma Right Side

Group B will receive PRP on right side of scalp and placebo (saline solution) on left side of scalp.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Female ≥18 years of age at baseline visit.
• Documentation of androgenic alopecia diagnosis as evidenced by one or more clinical features
• Not currently on any treatment for alopecia, or has undergone 2-week washout period if recently on medication(s) for alopecia
• Written informed consent obtained from subject and ability for subject to comply with the requirements of the study

Exclusion Criteria

• Pregnant or breastfeeding
• Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
• Have an infection, metastatic disease or certain skin conditions (ie. Psoriasis) which could worsen or spread with injections
• Diagnosed with a blood or bleeding disorder
• Diagnosed with anemia
• Currently on anticoagulant therapy

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Wake Forest University Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Rita Pichardo, MD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University School of Medicine, Department of Dermatology

Locations

Wake Forest University Baptist Health

Winston-Salem, North Carolina, United States

Countries

United States

Central Contacts

Research Coordinator

Role: CONTACT

irichard@wakehealth.edu

336-716-2903

Other Identifiers

IRB00045844

Identifier Type: -

Identifier Source: org_study_id