Effectiveness of Moyo Device on Intrapartum Detection of Abnormal Fetal Heart Rate: A Randomized Controlled Trial in Ethiopia
Not Applicable
- Conditions
- Pregnancy and Childbirth
- Registration Number
- PACTR202305607000259
- Lead Sponsor
- aerdal Foundation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 2518
Inclusion Criteria
Participants with an estimated gestational age of =37 weeks
- Participants with =4 cm cervical dilatation at admission
Exclusion Criteria
-Participants scheduled for cesarean section (CS)
-Participants with multiple pregnancies
-Participants with abnormal FHR on admission i.e. absent; FHR<110 or FHR>160 beats/minutes (BPM)or undetectable
-Participants with common pregnancy complications
-Participants with precipitous delivery
-Participants with =9 cm cervical dilatation at admission.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method