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Evaluation of an Oral Hair Supplement to Improve Hair Strength and Support Growth in Women and Men

Hair Thinning Clinical Trial

Official title:
A Single-Center Prospective Evaluation of an Oral Hair Supplement to Improve Hair Strength and Support Growth in Women and Men With Self-Perceived Hair Thinning

Clinical Trial Summary

A single-center, open-label, prospective study to demonstrate the efficacy of an oral supplement to improve the strength and support the growth of thinning hair in men and women with self-perceived hair thinning.

Clinical Trial Description

Female and male subjects will be enrolled in this single-site, open-label, prospective, interventional study evaluating 5 treatment regimens to improve the appearance of thinning hair. All treatment regimens are commercially available nutraceutical hair growth supplements. 50 subjects will be enrolled into each of the 5 supplement groups. Subjects will undergo a baseline, 90 day, and 180 day visit and will have compliance phone calls at Days 45 and 135. Study assessments will include a dermatologist investigator hair assessment, a hair pull test, light microscope hair shaft diameter assessment, and a subject questionnaire. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06362941
Study type Interventional
Source Nutraceutical Wellness Inc.
Contact Emily Hu
Phone 1-888-508-3471
Email emily.hu@nutrafol.com
Status Recruiting
Phase N/A
Start date May 20, 2024
Completion date March 30, 2025
View Details
See also
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