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 @ 7:52 PM
Ignite Modification Date:
2025-12-24 @ 7:52 PM
NCT ID:
NCT03122704
Eligibility Criteria:
\* Inclusion Criteria:
To be eligible for enrolment into this trial, subject must fulfil all of the following criteria, unless specified otherwise
* Being conceived through IVF
* Moderate uterine contractions (2 contractions per 10 minutes, duration \< 30 seconds)
* 20 0/7 to 36 6/7 weeks of gestation
* Intact membrane
* Cervical dilation ≤ 3 cm
* Willing to participate into the study
* Exclusion Criteria:
To be eligible for enrolment in this study each subject must not meet any of the following criteria:
* Having had intercourse during 24 hours before
* Being suspected of amniotic leakage
* Rupture of membrane identified by direct observation through speculum examination of amniotic fluid flow from cervix
* Vaginal bleeding
* Being suspected of placenta abruption, placenta previa
* Having been treated with antibiotics within 1 week before
* Vaginal douche within 48 hours before
* Having used vaginal medicines during 48 hours before
* Having vaginal ultrasound shortly before
* Urine culture positive with GBS
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT03122704
Study Brief:
Protocol Section:
NCT03122704