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 @ 3:14 PM
Ignite Modification Date:
2026-03-26 @ 3:14 PM
NCT ID:
NCT07446361
Eligibility Criteria:
Inclusion Criteria:
* Female trial participants aged from 30 to 70 years.
* Trial participants who are regular users of anti-aging cosmetic products.
* Trial participants presenting with:
* Wrinkle visibility score ≥3 and ≤6 on a 10-point visual scale.
* Fine lines visibility score ≥3 and ≤6 on a 10-point visual scale.
* Crow's feet wrinkle score ≥2 and ≤4 on the L'Oréal Atlas (volume 1 caucasian type).
* Skin radiance score ≥3 and ≤6 on a 10-point visual scale.
* Plumpness score ≥3 and ≤6 on a 10-point visual scale
Exclusion Criteria:
* Trial participants who are pregnant, breastfeeding, or planning to become pregnant during the study period.
* Trial participants who are currently participating in another facial clinical study or who have participated in such a study within 1 month that may interfere with the study outcomes.
* Trial participants presenting with current flaring or severe inflammatory acne or any active dermatological condition that, in the investigator's opinion, could interfere with study assessments.
* Trial participants who have undergone ablative laser treatments, microneedling, chemical peels, dermabrasion, non-ablative laser, intense pulsed light (IPL), or injectable procedures within the last 12 months from the day of screening.
* Trial participants who have undergone biostimulation procedures in the past 6 to 9 months from the day of screening
* Trial participants with a known allergy to any component of the investigational product(s), comparator product(s), or additional products used in the study.
* Trial participants presenting with any medical or dermatological condition that, in the investigator's opinion, may compromise trial participant safety or interfere with study conduct or evaluation.
* Trial participants who are unable or unwilling to comply with the study requirements and instructions.
* Trial participants who are unable to provide written informed consent.
* Trial participant with clinically significant history of alcoholism or drug abuse;
* Trial participant who are employees of MSCR or Sponsor
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
30 Years
Maximum Age:
70 Years
Study:
NCT07446361
Study Brief:
Protocol Section:
NCT07446361