An effectiveness study of a continuous approach from routine intrapartum care to emergency obstetric care on reducing severe maternal outcomes through nation-wide rollout in Lao PDR
Not Applicable
- Conditions
- Severe pre-eclampsia, eclampsia, postpartum hemorrhage, perinatal maternal infection, and other maternal severe outcome cases
- Registration Number
- JPRN-jRCT1090220328
- Lead Sponsor
- niversity of Tokyo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- PENDING
- Sex
- Female
- Target Recruitment
- 576
Inclusion Criteria
Women who was diagnosed as pre-eclampsia, eclampsia, postpartum hemorrhage, perinatal infection or other maternal complication in the target hospitals within the study period
Exclusion Criteria
None
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Risk of severe maternal outcomes among those with complications
- Secondary Outcome Measures
Name Time Method Quality of care for severe pre-eclampsia, eclampsia, postpartum hemorrhage