ConditionLabour
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorPak Emirates Military Hospital
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Design model
Parallel
Treatments tested in this trial
WHO Labour Care Guide
Other interventionLabour will be monitored using WHO Labour care guide
Partogram
Other interventionLabour will be monitored using partogram
Treatment groups
174 Participants
are divided into 2 treatment groupsGroup A: Group AExperimental treatment 1 intervention
Group B: Group BPlacebo comparator 1 intervention
Trial outcomes
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.
Time frame
24 hoursLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
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