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Outcomes of Delivery in Primigravida

Study of Outcomes of Delivery in Primgravida

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07075848
Enrollment
200
Registered
2025-07-20
Start date
2025-09-01
Completion date
2028-01-01
Last updated
2025-07-24

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

Conditions

Vaginal Delivery

Brief summary

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

Detailed description

The significance of auditing delivery care for primigravida women lies in their heightened vulnerability to complications such as prolonged labor, fetal distress, and higher rates of cesarean sections. Studies have shown that primigravida women often experience higher levels of fear and anxiety related to childbirth, which can influence their labor progression and overall birth experience. By systematically evaluating the care provided to this group, healthcare institutions can implement targeted interventions to enhance outcomes and patient satisfaction.

Interventions

PROCEDUREvaginal delivery

follow up of progress of labour

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Primigravida women admitted for delivery at the hospital * Singleton pregnancies. * Gestational age ≥ 28 weeks (to exclude preterm deliveries before viability). * Willingness to participate.

Exclusion criteria

* • Multiparous women. * Multiple pregnancies. * Women who decline to participate. * Deliveries occurring outside the specified study period.

Design outcomes

Primary

MeasureTime frame
The rate of vaginal delivery in cases24 hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026