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Recruiting NCT04728048

Dural Puncture Epidural VS Standard Epidural on Physician Top-ups During Labour Analgesia

Trial Parameters

Condition Obstetric Pain
Sponsor Ciusss de L'Est de l'Île de Montréal
Study Type INTERVENTIONAL
Phase N/A
Enrollment 130
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2021-01-19
Completion 2025-06
Interventions
Dural puncture epiduralStandard epidural

Brief Summary

The purpose of this prospective randomized controlled study is to compare the number of physician top-up interventions during the first stage of labour between two different neuraxial analgesia techniques : the dural puncture epidural and the standard epidural.

Eligibility Criteria

Inclusion Criteria: 1. Healthy pregnant women (ASA 1 and 2) requesting epidural analgesia during labour. 2. Primiparous and multiparous parturients at term gestation (37 to 42 weeks). 3. Women 18 years old and older. 4. Administration of epidural analgesia between 7am and 4pm on weekdays. 5. Singleton and vertex presentation foetus. 6. Cervical dilatation ≤ 5 cm. 7. BMI ≤ 40. 8. French speaking Exclusion Criteria: 1. Pregnancy diseases such as gestational hypertension, preeclampsia and gestational diabetes. 2. Contraindications to neuraxial analgesia: thrombocytopenia \< 70 x 109/L, spinal cord anomalies, anticoagulation therapy, etc. 3. Known important fetal anomalies. 4. Allergy to any of the medications used in the study. 5. Suspected chorioamnionitis with spontaneous premature rupture of membranes (PROM). 6. Difficulty understanding and speaking French.

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