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Study to Evaluate Xtresse Serum in Individuals With Thinning Hair

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Trial status changed: Enrolling by Invitation → Active, Not Recruiting
    • Study sites: 4 to 3
    v6
  2. Study sites revised (4)v5
  3. Enrollment target: 60 to 40
    • Primary and study completion dates: Aug 2026 to Mar 2027
    • Study sites: 3 to 4
    v4
  4. Start date changed from estimate of Nov 2025 to Dec 17, 2025v3
  5. Trial status: Not Yet Recruiting to Enrolling by Invitation
    • Start date: Dec 2025 to Nov 2025
    • Site contacts updated at 3 of 3 sites
    v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this study is to determine how safe and effective it is to improve hair growth by applying a serum daily on the scalp of men and women with thinning hair. The main aims of this trial are: 1. To confirm using photographic analysis, changes in the quality, volume, and thickness of hair. 2. To gauge patient satisfaction with hair changes and application process. 3. Monitor and report any adverse events associated with the daily usage of Xtressé serum. Participants who qualify will complete 7 visits after voluntary consent has been given. Participants will be given 9 bottles of serum to use during the study. The product will be applied daily over a 9-month period. Photographs and scalp analysis will be performed at each visit to measure changes in hair volume, thickness, and growth. Participants will complete a survey in the middle and at the end of the study.
Trial Details
NCT Number NCT07228156
Lead Sponsor Restore Biologics Holdings, Inc. dba Xtressé
Conditions
(from sponsor)		 Thin Hair, Hair Loss, Alopecia, Thinning Hair
Related terms Alopecia
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov