- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03376581
The Utility of Platelet Rich Plasma in Hair Loss
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Early Phase 1
Contacts and Locations
Study Locations
-
-
California
-
Irvine, California, United States, 92697
- University of California, Irvine, Department of Dermatology, Dermatology Clinical Research Center, Hewitt Hall
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Prospective treatment
|
Blood drawn from each participant will be spun down to separate platelets.
Platelets will be injected into that patient's scalp.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hair density to measure the efficacy of treatment
Time Frame: 6 months
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hair count (number of hairs/0.65 cm2)
Time Frame: 6 months
|
6 months
|
|
Terminal hair density
Time Frame: 6 months
|
6 months
|
|
Anagen hair percentage
Time Frame: 6 months
|
6 months
|
|
Telogen hair percentage
Time Frame: 6 months
|
6 months
|
|
Anagen/telogen ratio
Time Frame: After 3 and 6 months
|
After 3 and 6 months
|
|
Changes in hair structure, diameter, and blood flow
Time Frame: 6 months
|
As measured by optical coherence tomography
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20163239
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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