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NCT Number: NCT07550439

Effect of World Health Organization Labour Care Guide On Reducing Cesarean Section Rates

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.

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

After approval from ethical review committee, total 174 women presenting in the inpatient Department of Obstetrics & Gynaecology, Pak Emirates Military Hospital, Rawalpindi, fulfilling the inclusion criteria will be selected. Informed consent will be taken from each woman. Age, gestational age, parity, height, weight and BMI will be noted. 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. Cesarean section will be noted in both groups. This all data including demographic data will be recorded on a specially designed proforma

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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.

Exclusion criteria

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.

Treatment and study plan

WHO Labour Care Guide

Other

Labour will be monitored using WHO Labour care guide

Partogram

Other

Labour will be monitored using partogram

Primary outcomes

  1. Frequency of Cesarean Section

    Time frame: 24 hours

    To determine the frequency of caesarean section between World Health Organization Labour Care Guidelines versus partograph monitoring of labour.

Study contacts

Contact information is provided by the study sponsor or research team.

Dr Sana Murtaza, MBBS

CONTACT

[email protected]

+92 333 666188 ext. +92

Sponsors and collaborators

Lead sponsor

Pak Emirates Military Hospital

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 24, 2026
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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