Clinical Trial

Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women

Recruiting
View on ClinicalTrials.gov →
Summary
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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2024-08-26; most recent amendment 2026-04-07.
Status change: Not Yet Recruiting → Recruiting 2024-09-25
Trial Details
NCT Number NCT06580327
Lead Sponsor Holy Family Hospital, Nazareth, Israel
Conditions Breakthrough Pain
Enrollment 186 participants
Start Date 2024-09-25
Primary Completion 2026-11 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-04-13