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The Utility of Platelet Rich Plasma in Hair Loss

The Utility of Platelet Rich Plasma in Hair Loss

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03376581
Enrollment
30
Registered
2017-12-18
Start date
2017-11-28
Completion date
2019-02-20
Last updated
2024-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Androgenetic Alopecia

Brief 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.

Interventions

PROCEDUREPlatelet rich plasma

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

Sponsors

University of California, Irvine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
Hair density to measure the efficacy of treatment6 months

Secondary

MeasureTime frameDescription
Terminal hair density6 months
Anagen hair percentage6 months
Hair count (number of hairs/0.65 cm2)6 months
Anagen/telogen ratioAfter 3 and 6 months
Changes in hair structure, diameter, and blood flow6 monthsAs measured by optical coherence tomography
Telogen hair percentage6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026