RegrowProtocol

Trial pipeline · NCT06926023

1550nm Non-ablative Fractional Vs 1927nm Thulium Fractional Laser for the Treatment of Female Pattern Hair Loss

Not applicable Not yet recruiting status last verified 2025-04

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
NCT06926023
Lead sponsor
Goldman, Butterwick, Fitzpatrick and Groff (other)
Registered condition naming hair loss
Female Pattern Baldness
Official title
A Prospective, Randomized, Evaluator-blind, Clinical Trial Evaluating the 1550nm Non-ablative Fractional or 1927nm Thulium Fractional Laser for the Treatment of Female Pattern Hair Loss

Interventions

  • Device1550nm non-ablative fractional laser
  • Device1927 thulium fractional laser

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
randomized
Masking
single
Primary purpose
treatment
Enrolment
10 participants (estimated)
Sites
1 location in United States

What it measures

  1. Change in hair count at a predefined 1cm x 1cm scalp location

    Time frame: Baseline and Day 180

  2. Change in hair density (hairs/cm) at the same predefined scalp area

    Time frame: Baseline and Day 180

  3. Change in terminal hair average diameter (in mm) at the predefined location

    Time frame: Baseline and Day 180

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
35 Years to 65 Years
Healthy volunteers
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
1 May 2025 (estimated)
Primary completion
30 November 2025 (estimated)
Study completion
31 December 2025 (estimated)
First posted
13 April 2025 (actual)
Last update posted
16 April 2025 (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: this record registers a primary completion to the day, so a day is what is shown. Where a sponsor registers only a month, only a month is shown.

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 NCT06926023 on ClinicalTrials.gov · All 157 trials in the pipeline