Induction of labor with Foley cathether or Misoprostol (INFORM)
Phase 4
- Conditions
- Health Condition 1: null- Women with preeclampsia
- Registration Number
- CTRI/2013/07/003859
- Lead Sponsor
- niversity of Liverpool
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 602
Inclusion Criteria
Women with an ongoing pregnancy with a live fetus in whom the decision has been made to induce vaginal delivery because of preeclampsia or uncontrolled hypertension. Women will be included irrespective of whether an intrapartum caesarean section on fetal grouns would be considered or not.
Exclusion Criteria
Women with prior caesarean sections
Those unable to give informed consent
Multiple pregnancy
History of allergy to misoprostol
Ruptured membranes
Chorioanaionitis (by clinical diagnosis)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method