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 @ 2:21 AM
Ignite Modification Date:
2025-12-25 @ 2:21 AM
NCT ID:
NCT02037334
Eligibility Criteria:
Inclusion Criteria:
* All pregnant women presenting at their mid pregnancy consultation (18+0 - 22+0 weeks of pregnancy) are eligible
* Signed informed consent after being informed is a prerequisite for enrollment.
Exclusion Criteria:
* Communication problems
* Missing consent
* Age\<18
* Active bleeding / Premature Rupture of Membranes (PROM)
* Active genital infection
* Known carrier of HIV or Hepatitis B or C
* Placenta praevia
* Müllerian anomalies
* known or suspected non-compliance, drug or alcohol abuse
* cerclage
* use of pessary
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
60 Years
Study:
NCT02037334
Study Brief:
Protocol Section:
NCT02037334