Alopecia Areata Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are a woman between 28 and 65 years old who feels your hair has been consistently getting thinner
- A doctor has assessed your hair loss as mild to moderate (using a standard hair loss scale called the Ludwig Scale, levels I or II)
- You have any skin tone (all skin types are welcome)
- You are willing to keep your current diet, medications, exercise habits, hair washing routine, and hair coloring habits the same for the whole study
- You are able and willing to attend regular study visits and use the study product as instructed
- You are willing to sign a consent form, including allowing photos to be taken as part of the study
- If you could become pregnant, you have a negative pregnancy test at the start and agree to use a reliable form of birth control throughout the study (such as the pill, implant, injection, patch, IUD, condom, diaphragm, abstinence, or a partner who has had a vasectomy)
Who may not be able to join:
- You are pregnant, breastfeeding, or planning to become pregnant
- You have changed your hormone therapy (such as HRT or hormonal medications) in the last 6 months or plan to during the study
- You have used medical hair loss treatments such as Minoxidil, Dutasteride, Finasteride, or laser/light therapy for the scalp in the past 3 months or plan to during the study
- You have had micro-needling, PRP injections, or similar scalp treatments in the past 6 months or plan to during the study
- You have taken GLP-1 medications (such as Semaglutide/Ozempic) in the past 6 months or plan to during the study
- You have an uncontrolled health condition (such as a thyroid condition or anemia) that could affect the study results
- You have a known allergy or sensitivity to any ingredient in the study product
- The study doctor believes you may be unable or unwilling to follow the study rules and complete the study
- You have any other health condition or finding that the study doctor believes would make it unsafe or unsuitable for you to participate (confirm with trial site)
- You have taken part in a trial involving an experimental drug, medical device, or biologic treatment within the past 12 weeks
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Danielle Leavitt, Restore Biologics Holdings, Inc. dba Xtressé
Phone: 305-933-6716
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Increase in hair density (hairs per cm²) measured as the within-subject change from baseline to Month 3, assessed via Canfield HairMetrix® phototrichogram analyses.; Increase in hair density (hairs per cm²) Measured as the within-subject change from baseline to Month 9, assessed via Canfield HairMetrix® phototrichogram analyses.; Participant self-assessment of hair growth and satisfaction, collected via validated questionnaires.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.