New labor monitoring tool tested against old standard
NCT ID NCT07445373
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will compare the WHO Labour Care Guide with the older modified partograph to see which one helps doctors and nurses monitor labor better. About 114 women in active labor will be randomly assigned to one of the two monitoring methods. The goal is to see if the new guide leads to shorter labor, fewer C-sections, and healthier babies.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 114 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 40 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patient aged 20 to 40 years . * gestational age 37 to 42 weeks as per LMP. * parity UpTo 4 * singketon pregnancy on ultrasound * patient presenating In labor as per operational definitons Exclusion Criteria: * patients with breech presenation * pregnant women in whom trial of labor given outside the hospital, * women with complications like gestational diabetes,antepartum hemorrhage,severe preeclampsia/eclampsia and medical disorders complicating the pregnancy * premature rupture of membranes
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Khyber teacher hospital
Peshawar, Khyber Pakhtunkhwa, 25000, Pakistan
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