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 @ 1:50 PM
Ignite Modification Date:
2025-12-24 @ 1:50 PM
NCT ID:
NCT03862495
Eligibility Criteria:
Inclusion Criteria:
1. pregnant women on their first visit to the hospital (regardless of gestational age);
2. aged 18 or above;
3. agree to participate and sign an informed consent.
Exclusion Criteria:
1. systemic or topical vaginal antibiotics use within 2 weeks prior to the first perinatal visit;
2. comorbidities that are known to be related to adverse pregnancy outcomes (e.g., diabetes and hypertension);
3. diagnosed adverse pregnancy outcomes at recruitment (e.g., stillbirth); Women with a previous history of CT or NG and women with a prior adverse outcome will not be excluded. Instead, the investigators will conduct sub-analysis and check whether the intervention has different effects on different groups of pregnant women.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03862495
Study Brief:
Protocol Section:
NCT03862495