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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03376581
Other study ID # 20163239
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date November 28, 2017
Est. completion date February 20, 2019

Study information

Verified date February 2024
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Platelet rich plasma (PRP) is an autologous preparation of human plasma with high concentration of platelets. Platelets release numerous growth factors, which stimulate cell proliferation and differentiation. The purpose of this research is to investigate the potential of PRP injection for treatment of hair loss. Clinical outcomes will be assessed by noninvasive techniques including dermoscopy, multiphoton microscopy, optical coherence tomography, optical Doppler tomography and multispectral imaging.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 20, 2019
Est. primary completion date February 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria: - Over 18 years of age - Ability to understand and carry out instructions - Diagnosed with alopecia Exclusion Criteria: - Inability to understand and.or carry out instructions - Pregnant women - Use of any topical medication (such as minoxidil or any other solution for hair growth), oral medication (finasteride, dutasteride, or antiandrogens), laser therapy, or chemotherapy, within the preceding 4 weeks. - Personal medical history of bleeding disorders - Personal medical history of platelet dysfunction syndrome - Anti-coagulation therapy or nonsteroidal anti-inflammatory drugs in the last 1 week.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Platelet rich plasma
Blood drawn from each participant will be spun down to separate platelets. Platelets will be injected into that patient's scalp.

Locations

Country Name City State
United States University of California, Irvine, Department of Dermatology, Dermatology Clinical Research Center, Hewitt Hall Irvine California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Irvine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hair density to measure the efficacy of treatment 6 months
Secondary Hair count (number of hairs/0.65 cm2) 6 months
Secondary Terminal hair density 6 months
Secondary Anagen hair percentage 6 months
Secondary Telogen hair percentage 6 months
Secondary Anagen/telogen ratio After 3 and 6 months
Secondary Changes in hair structure, diameter, and blood flow As measured by optical coherence tomography 6 months
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