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 @ 12:17 PM
Ignite Modification Date:
2025-12-24 @ 12:17 PM
NCT ID:
NCT02633761
Eligibility Criteria:
Inclusion Criteria:
* Demised fetus of between 14 to 28 weeks duration confirmed by ultrasound
* Have no contraindications to study procedure, according to provider
* Be able to consent to procedure, either by reading consent document or by having consent document read to her
* Be willing to follow study procedures.
Exclusion Criteria:
* Allergies or other contraindications to the use of mifepristone or misoprostol;
* Placental abruption with active hemorrhage,
* Complete placenta previa, extreme uterine structural anomalies, or other contradictions to vaginal delivery of the fetus;
* Presentation in active labor (moderate to severe contractions every 10 minutes or less);
* Transmural uterine scars;
* Four or more previous deliveries.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
64 Years
Study:
NCT02633761
Study Brief:
Protocol Section:
NCT02633761