Platelet-rich Plasma for Eyebrows

Eyebrow Hypotrichosis Clinical Trial

Official title:

A Pilot Clinical Trial Investigating the Effect of Autologous Platelet-rich Plasma in Subjects With Mild to Moderate Eyebrow Hypotrichosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04018859
• Other study ID #: STU00207701
• Status: Recruiting
• Phase: Phase 2
• Start date: September 25, 2019
• Est. completion date: December 2024

Study information

• Verified date: March 2024
• Source: Northwestern University
• Contact: Alejandra Onate, M.S.
• Phone: 312-503-5944
• Email: onate[@]northwestern.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of autologous platelet-rich plasma (PRP) in the treatment of mild to moderate eyebrow hypotrichosis.

This is a randomized clinical trial to evaluate the effect of autologous platelet rich plasma in subjects with mild to moderate eyebrow hypotrichosis. Approximately 40 subjects will be randomized to receive platelet-rich plasma (PRP) or saline injections. The study is designed as an 9-month study. This study was a pilot study designed to determine feasibility of this procedure.

Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be considered for enrollment.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: December 2024
• Est. primary completion date: December 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

1. Males or females 18-85 years old.

2. Subjects are in good health as judged by the investigator.

3. Patients with mild to moderate eyebrow hypotrichosis (modified GEyA grades of 3 and 4 at the time of screening, see Appendix A).

4. Those who have less eyebrows and therefore, desire to enhance eyebrows (modified GEyA grades of 3 and 4 at the time of screening, see Appendix A).

5. Subjects who are willing and have the ability to understand and provide informed consent for participation in the study and are able to communicate with the investigator

Exclusion Criteria:

1. Patients with uncontrolled systemic disease (including alopecia areata or any other form of alopecia) which could inhibit hair growth

2. Patients with thrombocytopenia, platelet dysfunction, hypofibrinogenemia, anemia, cancer, active infections with Pseudomonas, Klebsiella, or Enterococcus, history of trichotillomania, thyroid diseases, eye diseases, atopic dermatitis, seborrheic dermatitis, lupus erythematosus, scleroderma, leprosy, or syphilis.

3. Patients who have started used agents that may affect eyebrow hair growth (e.g. minoxidil or bimatoprost) within 6 months of screening. Patients who have been using agents that may affect eyebrow hair growth for at least 12 months may be included if the patient agrees to continue their current dosing regimen for the duration of the study.

4. Known disease, infection, or abnormality in the treatment area or hair shaft

5. Patients with tattoos, scars, hyperpigmentation, or other features which could prevent accurate evaluation of hair growth in the eyebrow area.

6. Evidence of another skin condition affecting the treatment area that would interfere with clinical assessments

7. Unwilling to refrain from washing face or using face care products 24 hours before and after treatment visits

8. History of a clinically significant hematologic disorder as determined by the investigator.

9. Subjects currently receiving anticoagulant or anti-platelet therapy.

10. Subject is known to be HIV positive.

11. Known genetic disorders affecting fibroblasts or collagen, such as achondroplasia, osteogenesis imperfecta, etc.

12. Pregnant or breast feeding

13. Uncooperative patients or patients with neurological disorders who are incapable of following directions or who are predictably unwilling to return for follow-up examinations.

14. Subjects who are unable to understand the protocol or give informed consent (including non-English speaking patients).

Related Conditions & MeSH terms

• Eyebrow Hypotrichosis
• Hypotrichosis

Intervention

Device:
• Platelet Rich Plasma Prep System
intradermal injections of platelet rich plasma to the eyebrows

Drug:
• Saline
intradermal injections to the eyebrows

Locations

Country	Name	City	State
United States	Northwestern University	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical change of eyebrow hypotrichosis, as determined by scoring photographs		Baseline to 6 months