Clinical Trial

Integrated Intrapartum Supportive Care and Pushing Strategies in Women Receiving Low-Dose Epidural Analgesia

Recruiting
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Record status
This record was last updated June 23, 2026 (before its estimated July 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
This prospective, three-arm, non-randomized quasi-experimental study aims to evaluate integrated intrapartum supportive care combined with different pushing strategies among women at 37-42 weeks of gestation who receive low-dose epidural analgesia. Participants receive integrated intrapartum supportive care combined with spontaneous pushing, integrated intrapartum supportive care combined with immediate pushing, or routine intrapartum care combined with immediate pushing. The primary outcomes are the durations of the first and second stages of labor. Secondary outcomes include mode of birth, obstetric interventions, maternal outcomes, and neonatal outcomes.
Trial Details
NCT Number NCT07663500
Lead Sponsor National Taipei University of Nursing and Health Sciences
Conditions Labor, Obstetric, Epidural Analgesia, Obstetric, Labor Duration
Enrollment 159 participants
Start Date 2025-06-10
Primary Completion 2026-07-31 (estimated)
Study Completion 2026-07-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-23