An observational study in Vaginal Delivery, sponsored by Assiut University. Not yet recruiting. Open to female participants. Per ClinicalTrials.gov, last updated 2025-07-24.
Sponsored by Assiut University · Observational
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
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.
Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.
Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Primigravida come in labour
Exclusion Criteria:
Multiparous women.
Procedure: vaginal delivery
follow up of progress of labour
The rate of vaginal delivery in cases
Time frame: 24 hours
No study locations are listed for this record.
This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.
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Assiut University