Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women
Recruiting
N/A
Interventional Study
Breakthrough Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 186 (estimated)
- Sponsor
- Holy Family Hospital, Nazareth, Israel · Other
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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 m…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. multiparous women
2. Term pregnancy
3. Singleton
4. Vertex presentation
5. Latent phase (cervical dilatation less than 6 cm)
6. Epidural analgesia request
7. Visual Analogue Scale score greater than 40
Exclusion Criteria:
1. Estimated fetal weight greater than 4.0 kg
2. Int…
Contacts