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Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Dec 2025 to Nov 2026
    • Study completion date: Mar 2026 to Dec 2026
    v4
  2. Primary completion date: Aug 2025 to Dec 2025
    • Study completion date: Aug 2025 to Mar 2026
    v3
  3. Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Start date: Aug 2024 to Sep 25, 2024
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 1 of 26 entries
    • Site details revised
    • Study title expanded, about 1 word
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this randomized controlled trial is to examine the impact of programmed intermittent bolus epidural analgesia technique on the incidence of breakthrough pain during labor in multiparous women compared to continuous epidural infusion. multiparous women will randomly be divided during labor into two groups; study group will receive mix of Bupivacaine and fentanyl once (bolus) every 60 minutes; the control group will receive continuously the same dose during an hour, until delivery.
Trial Details
NCT Number NCT06580327
Lead Sponsor Holy Family Hospital, Nazareth, Israel
Conditions
(from sponsor)		 Breakthrough Pain
Related terms Breakthrough Pain
Enrollment 186 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov