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Ultrasonography and Health Education Can Reduce the Unnecessary Caesarean Section in Bangladesh

H

Hiroshima University

Status

Enrolling

Conditions

Increase Antenatal Care
Increase Institutional Delivery
Reduce Unnecessary Caesarean Section

Treatments

Diagnostic Test: Ultrasonograpgy

Study type

Interventional

Funder types

Other

Identifiers

NCT05135026
2021/OR-NSU/IRB/0804

Details and patient eligibility

About

A caesarean section (C/S) is a surgical procedure performed to prevent difficulties during childbirth. World Health Organization considered the standard rate for the C/S would be between 10% and 15%. However, since 2000 the rate of C/S was increasing globally, and it became about twofold from 12.1% to 21.1% in 2015.

In Bangladesh, C/S continued to increase from 8% (2007) to 33% (2017). Medically unnecessary C/S was estimated about 77% of all C/S in 2018, and it was increased from 66% since 2016. In Bangladesh, unnecessary C/S observed 9.0% and 3.2% C/S done due to avoid labour pain and 5.8% for the convenience of the mother. The economic burden of each C/S is average USD 612 and unfortunately, each patient spends this amount of money from out of pocket. Aim of this study is to do ultrasonography and health education can reduce unnecessary caesarean section among pregnant women compared to control group in a resource poor setting.

Investigators will conduct this randomized controlled trial (RCT) at Dhaka and Sir Salimullah Medical College & Hospital, and two rural Upazila Health Complexes (Savar Upazila Health Complex and Munshigonj General Hospital). Investigators will randomly select one urban hospital from two urban hospitals and one rural hospital from two rural hospitals for the intervention. The other one urban and one rural hospital will be assigned as control hospitals. One research staff, who will not involve any of the research activity of this trial, will do this randomization. Pregnant mothers will be identified and recruited during their routine antenatal visits. Pregnant mothers receive 2 USG during their routine ANC visits at 1st visit of 8-12 weeks and 4th visit of 36-38 weeks. In the intervention centres, Investigators will perform additional 4 ANC visits at 20, 30, 36 and 40 weeks (total 8 visits) and USG additional 2 times during the 2nd visit of 24-26 weeks and 5th visit of 34 weeks (2 routine USG + 2 USG in 3rd and 5th ANC visits and even more USG if needed + Health education; pictorial flip chart showing danger sign during pregnancy and potential risks for unnecessary caesarean delivery to increase awareness for safe delivery) for all the enrolled pregnant mothers. In the control centres, Investigators will collect information from the pregnant mothers.

Investigators are expecting the pregnant women who will receive antenatal care with ultrasonography and health education will have reduced number of unnecessary C/S compared to control group who will not receive those.

Enrollment

288 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. All the pregnant mothers irrespective of age who will be attending the designated hospitals/health complex.
  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.)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

288 participants in 2 patient groups

Control Group (CG)
No Intervention group
Description:
Usual care
Intervention Group (IG)
Experimental group
Description:
In the intervention hospitals, we will perform USG additional 2 times during the 3rd visit of 24-26 weeks and 5th visit of 34 weeks (2 USG and even more USG if needed + additional 4 ANC + Health education; pictorial flip chart showing danger sign during pregnancy and potential risks for unnecessary caesarean delivery to increase awareness for safe delivery) for all the enolled pregnant mothers.
Treatment:
Diagnostic Test: Ultrasonograpgy

Trial contacts and locations

1

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Central trial contact

Mohammad Delwer Hossain Hawlader, MBBS MPH PhD; Michiko Moriyama, RN MSN Ph.D

Data sourced from clinicaltrials.gov

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