Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorHoly Family Hospital, Nazareth, Israel

About this trial

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.

Eligibility criteria

Qualifiers

multiparous women

Term pregnancy

Singleton

Vertex presentation

Disqualifiers

Estimated fetal weight greater than 4.0 kg

Intra uterine fetal death

Drug sensitivity

Trial design

Treatments tested in this trial

  • programmed intermittent Bolus epidural analgesia
  • continuous epidural infusion

Treatment groups

186 Participants
are divided into 2 treatment groups