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Clinical Trials/CTRI/2019/04/018827
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
niversity of Liverpool

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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