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Improving care of women during pregnancy, delivery and the period after delivery in the government health system

Not Applicable
Registration Number
CTRI/2023/02/049354
Lead Sponsor
Centre for Health Research and Development Society for Applied Studies
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

A pregnant woman who meets the following inclusion criteria may be enrolled at any stage of her pregnancy:

Women with confirmed pregnancy identified within the study catchment area through pregnancy surveillance and at study health facility

Exclusion Criteria

1. Decline to provide consent

2. Inability to provide informed consent

3. Less than 18 years of age

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maternal Outcomes: <br/ ><br>1. Maternal mortality & Severe maternal morbidity <br/ ><br>2. Maternal anemia <br/ ><br> <br/ ><br>Fetal and Neonatal outcomes <br/ ><br>1. Stillbirth <br/ ><br>2. 7-day neonatal mortality <br/ ><br>3. 28-day neonatal mortality <br/ ><br>4. Preterm birth <br/ ><br>5. Low birth weight delivery <br/ ><br>Timepoint: Maternal outcomes: During pregnancy, at delivery point and up to one-year post-delivery <br/ ><br> <br/ ><br>Fetal and Neonatal outcomes: At the time of delivery or up to 28 days of birth
Secondary Outcome Measures
NameTimeMethod
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