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
Qualifiers
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 design
Treatments tested in this trial
- vaginal delivery
Treatment groups
200 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov