EUCTR2016-003010-26-BE
Active, not recruiting
Phase 1
Hyperbaric Bupivacaine Versus Hyperbaric Prilocaine 2% for Cesarean Section Under Spinal Anesthesia: a Randomised and Controlled Clinical Trial
Centre Hospitalier Universitaire Saint Pierre , ULB0 sites100 target enrollmentDecember 6, 2017
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Parturients undergoing an elective caesarean section performed under spinal anaesthesia
- Sponsor
- Centre Hospitalier Universitaire Saint Pierre , ULB
- Enrollment
- 100
- Status
- Active, not recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •American Society of Anesthesiologists physical status (ASA) \< III
- •Age 18\-40 year
- •Body Weight \<110 kg
- •Height between 160 and 175 cm
- •Gestational age\>37 SA
- •Elective cesarean delivery
- •Singleton pregnancy
- •Non complicated pregnancy
- •Signed informed consent obtained prior to any study specific assessments and procedures
- •Are the trial subjects under 18? no
Exclusion Criteria
- •Twin pregnancy
- •History of 2 cesarean section or more
- •Diabetes and gestational diabetes
- •Placenta praevia
- •Congenital foetale abnormality
- •Intrauterine growth retardation
- •Patient in labour
- •Membrane rupture
- •Known allergy to local anaesthetics
- •Standard contraindications to neuraxial block.
Outcomes
Primary Outcomes
Not specified
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