Outcomes of Delivery in Primigravida
ConditionVaginal Delivery
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorAssiut University
About this trial
Primigravida women are a high-priority population due to their increased risk of obstetric interventions and adverse outcomes compared to multiparous women. Research indicates that first-time mothers account for a disproportionate number of emergency cesarean sections and instrumental deliveries, often due to factors such as inadequate labor support or failure to progress
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Primigravida women admitted for delivery at the hospital
Singleton pregnancies.
Gestational age ≥ 28 weeks (to exclude preterm deliveries before viability).
Willingness to participate.
Disqualifiers
• Multiparous women.
Multiple pregnancies.
Women who decline to participate.
Deliveries occurring outside the specified study period.
Trial population
Primigravida come in labour
Trial design
Design model
Other
Time perspective
Cross-sectional
Treatments tested in this trial
vaginal delivery
Procedure/Surgeryfollow up of progress of labour
Treatment groups
200 Participants
are divided into 1 treatment groupGroup A: study group1 intervention
Trial outcomes
Primary outcomes
1
The rate of vaginal delivery in cases
Time frame
24 hoursLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: