Condition: Breakthrough Pain · Sponsor: Holy Family Hospital, Nazareth, Israel
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 nulliparous women compared to continuous epidural infusion. Nulliparous 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.
This description comes directly from the study's public registry record.
Raed Salim, MD · +972544986960 · r.salim@hfhosp.org
Asmaa Masri Esmail, MD · +972544986960 · Asmaa.Masri94@gmail.com
Always discuss trial participation with your own doctor first.
| Holy Family Hospital | Nazareth, Israel | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06494280