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Clinical Trials/PACTR202404517245279
PACTR202404517245279
Not yet recruiting
Phase 1

Maternal And Fetal Outcome Of Planned Induction Of Labour Versus Caesarean Section For Severe Preeclampsia With Unfavourable Cervix At/Or Near Term

Buraimoh Jimoh0 sites120 target enrollmentJanuary 29, 2024
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ConditionsThe other condition include Hypertensive disorder in pregnancy

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
The other condition include Hypertensive disorder in pregnancy
Sponsor
Buraimoh Jimoh
Enrollment
120
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 29, 2024
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Buraimoh Jimoh

Eligibility Criteria

Inclusion Criteria

  • •My inclusion criteria included only consenting women with live singleton intrauterine pregnancy from 36 completed weeks to 42 completed weeks, diagnosed with severe preeclampsia in whom unfavourable cervix was the only indication for caesarean delivery.

Exclusion Criteria

  • •Patients with the following conditions were excluded from participating in the study:
  • •1\. Multiple gestations.
  • •2\. Spontaneous labour.
  • •3\. Foetal distress.
  • •4\.Eclampsia
  • •5\. Foetal anomaly.
  • •6\. Intrauterine growth restriction (IUGR).
  • •7\.Severe oligohydramnios
  • •8\.Pregnancies with other medical co\-morbidities like Diabetes Mellitus, Thyroid disease, and Sickle Cell
  • •9 Severe preeclampsia with gestational age less than 36 weeks

Outcomes

Primary Outcomes

Not specified

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