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Comparative Study Between Using WHO Labour Care Guide & Modified WHO Partograph

Comparative Study Between Using WHO Labour Care Guide & Modified WHO Partograph in Reducing Primary Cesarean Section in Primiparous Women in Active First Stage of Labour.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06537089
Enrollment
230
Registered
2024-08-05
Start date
2024-08-01
Completion date
2025-12-31
Last updated
2026-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor Onset and Length Abnormalities, 37 or More Completed Weeks of Gestation, First Birth

Keywords

labour Monitoring, primiparous

Brief summary

This randomized clinical trial is based on comparing the efficiency of modified WHO partographs vs. the new WHO labour care guide in monitoring and assessing the outcome of labour.

Detailed description

A group of primiparous women in first stage of labour will be randomized into two groups then monitored during first stage of labour. First group will be monitored by modified WHO partograph. The rest of participants will be monitored by WHO labour care Guide. The labour will be monitored regarding progress rate, mode of delivery.

Interventions

traditional partograph to properly manage first stage of labor

OTHERLCG guided labour interference

LCG as a new tool to make proper decision and management of first stage of labour

Sponsors

Hend Mahmoud Abdelghany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Primiparous women. * Term gestation between 37 and 40 weeks. * Maternal age from 18 -35 years * Body mass index BMI of 18.5 to 29.9 kg/m2 * Cephalic presentation. 6. Active first stage of labour

Exclusion criteria

* Women with any medical comorbidities, such as (hypertension, diabetes mellitus, renal disease, or pulmonary disease). * Women with presence of any obstetrical complications, such as preterm birth, multiple gestation, breech presentation, postdated pregnancy, or bad obstetrical history. * women who were given intrapartum epidural analgesia.

Design outcomes

Primary

MeasureTime frameDescription
Rate of primary caesarean sectionFirst and second stage of labournumber of women will undergo Caesarean section after monitoring, whether by Modified WHO partograph or a labour care Guide

Secondary

MeasureTime frame
Duration of active phase of first stage of labourFirst stage of labour
Duration of second stage of labourSecond stage of labour
need for oxytocin useFirst stage of labour

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026