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Using Ongoing Newborn Intervention Trials to Obtain Additional Data Critical to Maternal, Fetal and Newborn Health in a Harmonized Way

NCT01699945 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2258

Last updated 2016-10-31

No results posted yet for this study

Summary

The goal of this study is to generate unique information to guide improvements on interventions to reduce maternal and newborn mortality as well as prevent stillbirths.

The objective of this study is to determine the burden, timing, and causes of maternal deaths, stillbirths and neonatal deaths.

This will be an observational study where data will be collected retrospectively in the context of the ongoing study in Haryana, India.

Women of reproductive age living in the study area have already been enumerated for the parent studies. Active surveillance is being conducted for identifying pregnancies and deaths among women of reproductive age in the population through 3 monthly home visitations.

Verbal autopsies will be conducted for all deaths of women in the reproductive age, including those who died in pregnancy, childbirth and up to 42-60 days after childbirth. Verbal autopsy interviews will also be conducted for all stillbirths.

Conditions

  • Maternal Deaths
  • Neonatal Deaths
  • Still Births

Interventions

OTHER

This is an observational study being conducted as a substudy of antoher trial.

Sponsors & Collaborators

Principal Investigators

  • Sarmila Mazumder, PhD · CHRD, Society for Applied Studies

Eligibility

Min Age
15 Years
Max Age
49 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2016-01-31
Completion
2016-01-31

Countries

  • India

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01699945 on ClinicalTrials.gov