Effect of World Health Organization Labour Care Guide On Reducing Cesarean Section Rates
1 other identifier
interventional
174
0 countries
N/A
Brief Summary
After taking informed consent for participation in the study, all selected cases will be divided into two groups by lottery method. In group A, patients will receive care using WHO Labour Care Guide while in group B, patients will be monitored using WHO partograph.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 19, 2026
CompletedFirst Posted
Study publicly available on registry
April 24, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
April 24, 2026
April 1, 2026
6 months
April 19, 2026
April 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frequency of Cesarean Section
To determine the frequency of caesarean section between World Health Organization Labour Care Guidelines versus partograph monitoring of labour.
24 hours
Study Arms (2)
Group A
EXPERIMENTALIn group A, patients will receive care using WHO Labour Care Guide.
Group B
PLACEBO COMPARATORIn group B, patients will be monitored using WHO partograph.
Interventions
Eligibility Criteria
You may qualify if:
- All pregnant women in active phase of labour (\>5cm cervical dilatation) and gestational age of 37 weeks to 41 completed weeks (as assessed on LMP).
- Previous no caesarean section. Age 18-40 years. Both primiparous and multiparous. Both booked and unbooked.
You may not qualify if:
- Women with chronic hypertension (BP \>140/90 mmHg on 2 consecutive occasions). Pregnancy induced Hypertension: women with no history of hypertension (blood pressure \>140/90 mmHg on 2 consecutive occasions) and diagnosed in pregnancy.
- Gestational Diabetes mellitus: women with no history of diabetes mellitus (FBS \>110 mg/dl on 2 consecutive occasions) and diagnosed in pregnancy.
- Women who had a caesarean section in the latent phase of labour.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Officials
- PRINCIPAL INVESTIGATOR
Salma Nisar, MBBS, FCPS
Pak Emirates Military Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Registrar
Study Record Dates
First Submitted
April 19, 2026
First Posted
April 24, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
November 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
April 24, 2026
Record last verified: 2026-04