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Ultrasound and education may cut unnecessary C-Sections in bangladesh

NCT ID NCT05135026

Disease control Sponsor: Hiroshima University Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested if giving pregnant women extra ultrasounds and health education during checkups could reduce the number of unnecessary C-sections in Bangladesh. 288 pregnant women from urban and rural hospitals took part. The goal was to see if these extra services help women avoid C-sections that are not medically needed.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

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

288 people

The number who actually took part.

Started

Nov 2021

Finished

Dec 2025

Lead sponsor

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: 1. All the pregnant mothers irrespective of age who will be attending the designated hospitals/health complex in their first trimester. 2. We will include all pregnant mothers who will have/have not complication to see the delivery outcome with indication of normal delivery and CS. 3. Willing to participate in the study. Exclusion Criteria: 1. Not willing to participate. 2. Early Pregnancy with indication for C/S (co-morbidities, H/O previous C/S etc.) in their first trimester.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Increase antenatal care Increase institutional delivery Reduce unnecessary caesarean section

Contacts and locations

Locations

  • DMCH, SSMC, Munshiganj General Hospital and Bogra District Hospital

    Dhaka, Bangladesh