Can simple birth kits save lives in flood zones?
NCT ID NCT05640063
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This trial tests whether providing enhanced delivery and newborn kits, along with training for community health workers, can reduce perinatal deaths compared to standard kits in flood-affected districts of Sindh, Pakistan. Pregnant women in the intervention areas receive the enhanced kits for use at home or at health facilities, aiming to reduce delays in care. The study will measure perinatal mortality rates and specific causes of newborn and maternal deaths.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Enhanced delivery and newborn kits provided to pregnant women, along with training for community health workers and healthcare providers.
- What this could lead to
- If effective, this approach could reduce perinatal and maternal deaths in disaster-affected regions, offering a low-cost, scalable intervention for improving birth outcomes in similar settings.
- What could go wrong
- The trial is set in specific flood-affected districts, so results may not generalize to other contexts. Implementation challenges in crisis settings could also affect outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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2,400 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Dec 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pregnant women in the project sites living in the area till expected date of their delivery. Exclusion Criteria: * The individuals who would not consent to participate in the study voluntarily.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Aga Khan University
Karachi, Sindh, 74800, Pakistan
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