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 must be willing to sign a written agreement to follow the study rules (compliance consent).
- You must be willing to sign a written informed consent form for this specific study.
- You must be male.
- You must be between 18 and 45 years old.
- You must have been diagnosed with hair loss with low hair density, rated as mild to moderate (stages II, III, or IV on a standard hair loss scale called the Hamilton-Norwood scale).
- You must be willing to have a small area of hair (about 1–2 cm², roughly the size of a fingernail) shaved for the duration of the study.
- Your last participation in any clinical study about hair health must have ended at least 6 months before this study begins.
- You must have gone at least 30 days without using any specific hair treatments, using only a neutral (plain) shampoo during that time.
- You must agree not to use any other hair treatments — applied to the skin or taken by mouth — on the target area during the study period; if this becomes necessary, you would need to speak with the lead researcher first.
Who may not be able to join:
- People who have a gastrointestinal (digestive system) condition, such as diabetes, gastritis, Crohn's disease, celiac disease, stomach ulcers, or food intolerances.
- People who have other health conditions such as diabetes, high blood pressure, high cholesterol, or gallstones.
- People who are currently taking, or have taken in the last 3 months, certain medications that affect hair loss — such as Finasteride, Dutasteride, or Minoxidil — or any other medication that could affect the study results (confirm with trial site).
- People who have ever had any hair restoration procedure, including hair transplants, mesotherapy, or platelet-rich plasma (PRP) therapy.
- People who follow an unusual or restrictive diet, or who plan to change their eating habits during the study.
- People who are already taking part in another clinical study with a similar focus during the study period.
- People who are unable to fully understand the consent form or who may not be able to follow the study rules.
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
Phone: 96 187 45 82
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
Objective Evaluation of Hair Health Benefits After Six Months of Treatment; Total Terminal Count; Hair Density; Terminal Hair Density; Terminal Hair Proportion; Anagel and Telogen; Hair Mass; Median and Mean Hair Thickness; Hair length
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.