PACTR202404517245279Not yet recruitingPhase 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 enrollmentStarted: January 29, 2024Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 120
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 13 Year(s) to 18 Year(s) (—)
- Sex
- Female
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
- •10. Women with favourable cervical score
Investigators
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