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NCT03474718
Evaluating the Efficacy of Platelet-rich Plasma Therapy in the Treatment of Androgenic Alopecia
Conditions: Androgenic Alopecia
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: EARLY_PHASE1
Enrollment: 16
Sponsor: Wake Forest University Health Sciences
Location: Wake Forest University Baptist Health Winston-Salem North Carolina
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.
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
Source: ClinicalTrials.gov (NCT03474718). StuddyBuddy aggregates publicly available trial information.