NCT07550439

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
174

participants targeted

Target at P75+ for not_applicable

Timeline
7mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Study Progress3%
May 2026Dec 2026

First Submitted

Initial submission to the registry

April 19, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 24, 2026

Completed
7 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

April 24, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 19, 2026

Last Update Submit

April 19, 2026

Conditions

Keywords

Labour Care Guide

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

EXPERIMENTAL

In group A, patients will receive care using WHO Labour Care Guide.

Other: WHO Labour Care Guide

Group B

PLACEBO COMPARATOR

In group B, patients will be monitored using WHO partograph.

Other: Partogram

Interventions

Labour will be monitored using WHO Labour care guide

Group A

Labour will be monitored using partogram

Group B

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant females
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

  • Salma Nisar, MBBS, FCPS

    Pak Emirates Military Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Dr Sana Murtaza, MBBS

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: To determine the frequency of caesarean section between World Health Organization Labour Care Guidelines versus partograph monitoring of labour.
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