Eligibility Module

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: 2025-12-24 @ 9:43 PM
Ignite Modification Date: 2025-12-24 @ 9:43 PM
NCT ID: NCT04476732
Eligibility Criteria: Inclusion Criteria: * Individuals aged 15 and over * No known medical conditions that, in the investigator's opinion, may interfere with study participation. Exclusion Criteria: * Individuals who have been on any medication (including antibiotics, probiotics, prebiotics) that has caused a change in current skin composition of interest based on the opinion of the investigator. * Individuals with systemic antibiotic use within last 60 days. * Individuals with topical antibiotic use on the test sites within last 30 days * Individuals unwilling/unable to avoid topical antibiotics, systemic antibiotics, prebiotics, and probiotics during study. * No other interfering skin products should be used during duration of study. (Paraben-free \& phthalate-free personal product "safe" list will be provided for other uses during study period if needed). * Individuals unwilling or unable to undergo 1 week wash-in with paraben/phthalate-free products if needed in the opinion of the investigator. * Female volunteers who are pregnant or are actively breastfeeding or planning a pregnancy within two months. (There is no known concern for risk to fetus but pregnancy can alter the microbiome being studied) * Female volunteers who have started a new hormonal birth control agent or switched to a hormonal birth control agent within the past 60 days * Individuals using any interfering skin products in the opinion of the investigator within 2 weeks of enrollment into the study. * Individuals who have participated in any other clinical studies using the same test sites (face) in the past 14 days * Individuals with a known history of hypersensitivity to any ingredients to the cosmetic agent that is being assessed * Individuals who have history of a psychological illness or condition that would interfere with their ability to understand and follow the requirements of the study at the discretion of the investigator.
Healthy Volunteers: True
Sex: ALL
Minimum Age: 15 Years
Study: NCT04476732
Study Brief:
Protocol Section: NCT04476732