Outcomes of Delivery in Primigravida
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: vaginal delivery.
- Who it may be relevant to
- Registry conditions: Vaginal Delivery. Basic parameters: No limits · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Study of Outcomes of Delivery in Primgravida
Overview
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
- Procedure vaginal delivery
follow up of progress of labour
Primary outcome measures
- The rate of vaginal delivery in cases [Time frame: 24 hours]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07075848 · PGDA