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: 2025-12-25 @ 12:07 AM
Ignite Modification Date: 2025-12-25 @ 12:07 AM
NCT ID: NCT04973358
Eligibility Criteria: Inclusion Criteria: * 18 years of age or older: * with at least 20 permanent natural teeth, excluding crowns; * affiliated to a social security system; * having received information about the protocol and having given their free, informed and written consent. Exclusion Criteria: * with periodontitis in the month prior to inclusion; * with significant carious lesions deeply modifying the oral microbiota in the month prior to inclusion; * having undergone oral surgical treatment within 3 months prior to inclusion; * wearing orthodontic appliances; * having undergone periodontal procedures in the month prior to inclusion; * suffering from severe chronic pathologies deemed incompatible with study entry; * allergic to one of the swab components; * allergic to any of the components of the BUCCOTHERM mouthwash or the placebo; * on drugs that may cause gingival hypertrophy, such as Hydantoins (phenytoin), Dihydropyridines, Diltiazem or Ciclosporin; * Medications that can cause gingival bleeding (anticoagulants, antiplatelet agents and aspirin); * Antibiotic therapy or professional scaling in the month prior to inclusion; * having used oral or topical antibiotics, antiseptics and/or antifungals (e.g., mouthwash, dental gels, etc.) in the month prior to inclusion. * Subjects with poor written and spoken French language skills; * previously included in the BUCCOTHERM study; * simultaneously participating in another trial that may interfere with the conduct of the BUCCOTHERM study or in a period of exclusion after participation in another clinical study; * protected persons (adults under legal protection (legal guardianship, curatorship, tutorship), persons deprived of liberty, pregnant or breastfeeding women, women of childbearing age without effective contraception (estrogen-progestin treatments, IUD, tubal ligation), minors.
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Study: NCT04973358
Study Brief:
Protocol Section: NCT04973358