CTRI/2013/07/003859Not yet recruitingPhase 4
Induction of labor in preeclamptic women: a randomised trial comparing the Foley baloon catheter with oral misoprostol - INFORM
niversity of Liverpool0 sites602 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 602
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
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)
Investigators
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