Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-26 @ 3:19 PM
NCT ID:
NCT07433933
Eligibility Criteria:
Inclusion Criteria:
* Sex: Both (50% women; 50% men).
* Age: 18-65 years.
* Subjects with hair loss due to telogen effluvium or mild or incipient androgenic alopecia, in an 80/20 ratio.
* Degree of androgenic alopecia: Ludwig scale score I-II for women and Hamilton-Norwood scale score III-II for men.
* Telogen effluvium: Combing test.
* Subjects with all hair types (oily, combination, sensitive, etc.).
* Subjects with all scalp types (normal, sensitive, etc.).
* Agree to participate voluntarily in the study and provide written informed consent.
* Adequate level of understanding of the clinical study.
* Good health (physical and mental).
* Availability to attend visits to the research centres.
* No application of any product to the experimental area on the first day of the trial.
Exclusion Criteria:
* Individuals under 18 years of age.
* Pregnant or breastfeeding women.
* Injuries or infection in the test area.
* History of allergies to cosmetic products.
* Known allergies to product components.
* Sensitivity to any product component.
* Patients who have undergone recent surgery or treatments in the study area.
* Cancer patients.
* Volunteers currently taking antibiotics, antihistamines, corticosteroids, beta-blockers, retinoids, azelaic acid, or acne therapies, or whose treatment ended within 15 days prior to the start of the study. Participation in another clinical study.
* Use of or having used cosmetic products and/or oral or topical treatments for hair loss for at least 6 months.
* Hair cutting or dyeing during the study.
* Health problems, to be assessed by the specialist, that may compromise adherence to the study protocol.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT07433933
Study Brief:
Protocol Section:
NCT07433933