RegrowProtocol

Trial pipeline · NCT07224555

Study Evaluating Xtressé Gummy Supplement in Women With Self-Perceived Thinning Hair

Not applicable Enrolling by invitation status last verified 2025-11

A registered clinical trial, reproduced from its ClinicalTrials.gov record. Every value on this page is a field on that record. Nothing on this page is a finding, an assessment or a recommendation.

The registered record

Accession number
NCT07224555
Lead sponsor
Restore Biologics Holdings, Inc. dba Xtressé (industry)
Registered condition naming hair loss
Hair Thinning
Official title
Pilot Study to Evaluate the Efficacy and Safety of Xtressé™ Gummy-Based Nutraceutical Supplement in Women With Self-Perceived Thinning Hair

Interventions

  • OtherXtressé Hair Growth Gummies

Names and types as registered. The sponsors' free-text descriptions of these interventions are not reproduced: they are written by the party with an interest in the result, and reprinting them inside this site's layout would lend them this site's voice.

Design

Study type
interventional
Phase
Not applicable
Allocation
na
Masking
none
Primary purpose
treatment
Enrolment
60 participants (estimated)
Sites
4 locations in United States

What it measures

  1. Hair Density Changes measured by SOCAi

    Time frame: From enrollment to the end of the study at 4 months

  2. Within-subject increase in hair density assessed via Canfield HairMetrix® Phototrichogram Analysis

    Time frame: From enrollment to the end of treatment at 4 months

  3. Within-subject increase in hair thickness assessed via Canfield HairMetrix® Phototrichogram Analysis

    Time frame: From enrollment to the end of treatment at 4 months

Primary outcome measures only, as registered. What a trial chose to measure, and when, is the most informative thing about it that is knowable before it reports — a hair-count endpoint at 24 weeks and a patient-satisfaction endpoint at 12 weeks are not the same study.

Who can take part

Sex
female
Age
18 Years to 65 Years
Healthy volunteers
not accepted

A summary of three registered fields, not the eligibility criteria. The full inclusion and exclusion criteria, the recruiting sites and the study contacts are on the registry record, which is the only place they are maintained. This site has no relationship with this trial and cannot refer anyone to it.

Registered dates

Study start
27 March 2025 (actual)
Primary completion
December 2026 (estimated)
Study completion
March 2027 (estimated)
First posted
4 November 2025 (actual)
Last update posted
8 June 2026 (actual)

"Estimated" and "actual" are the registry's own labels: an estimated date is a plan, and plans move. A date is printed at the precision it was registered at: a primary completion registered as 2026-12 is a month, and rendering it as 1 December 2026 would invent a day the sponsor did not register.

Results

This trial has not reported results. ClinicalTrials.gov holds no results record for it. That is the ordinary state of a trial that is running or about to run, and it means there is nothing here to tell you about whether the intervention works — including nothing negative. If this page implied otherwise it would be wrong.

On this site

Guides covering the condition this trial is registered for. They are about published evidence; this page is about a registration, and the two do not overlap.

Where this came from

Read from the ClinicalTrials.gov API on 6 September 2026 and rebuilt into this page without alteration. ClinicalTrials.gov is a service of the U.S. National Library of Medicine and is the authority on this record; where this page and the registry disagree, the registry is right. This page is not affiliated with or endorsed by NLM or NIH, or with the sponsor of this trial.

Open NCT07224555 on ClinicalTrials.gov · All 157 trials in the pipeline