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 @ 3:45 AM
Ignite Modification Date:
2025-12-25 @ 3:45 AM
NCT ID:
NCT03749902
Eligibility Criteria:
Inclusion Criteria:
* • Ongoing pregnancies with a live fetus who require induction because of preeclampsia or hypertensionWomen will be included irrespective of whether an intrapartum caesarean birth on fetal grounds would be considered or not
* Women age ≥18 years
* Signed informed consent form
* Undergone cervical ripening with misoprostol if cervix initially unfavourable
* Decision to augment labour for inadequate uterine contractions despite ruptured membranes (either artificial or spontaneous as part of the induction process)s
Exclusion Criteria:
* Women with previous caesarean births
* Those unable to give informed consent
* Cervical ripening with agents other than misoprostol (e.g. Foley catheter, prostaglandins)
* Multiple pregnancy
* History of allergy to misoprostol
* Adequate uterine activity
* Pre- induction Ruptured amniotic membranes
* Frank chorioamnionitis (systemic illness with purulent vaginal discharge and uterine tenderness)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03749902
Study Brief:
Protocol Section:
NCT03749902