Outcomes of Delivery in Primigravida

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-01

Study Completion Date

2028-01-01

Brief Summary

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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

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Detailed Description

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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.

Conditions

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Vaginal Delivery

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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study group

vaginal delivery

Intervention Type PROCEDURE

follow up of progress of labour

Interventions

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vaginal delivery

follow up of progress of labour

Intervention Type PROCEDURE

Eligibility Criteria

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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.