CTRI/2019/04/018827
Recruiting
未知
A randomized trial comparing oral misoprostol alone with oral misoprostol followed by oxytocin in women induced for hypertension of pregnancy - MOLI
niversity of Liverpool0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity of Liverpool
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Ongoing pregnancies with a live fetus who are require induction because of preeclampsia or hypertension. Women will be included irrespective of whether an intrapartum caesarean section on fetal grounds would be considered or not
- •2\.Women age \>\=18 years
- •3\.Signed informed consent form
Exclusion Criteria
- •Women with previous caesarean sections
- •1\.Those unable to give informed consent
- •2\.Multiple pregnancy
- •3\.History of allergy to misoprostol
- •4\.Adequate uterine activity
- •5\.Frank chorioamnionitis (systemic illness with purulent vaginal discharge and uterine tenderness
Outcomes
Primary Outcomes
Not specified
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