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Clinical Trial Summary

The aim of this study is to compare effective analgesia with continuous wound infiltration of ropivacaine through multi-holed catheter or with morphine 100 mcg added intrathecally to spinal anesthesia, after elective Caesarean delivery.


Clinical Trial Description

Double blind, 3 groups

- Control group: Rachi 0,1 ml saline, Infusion 300ml saline

- Group rachi-morphine: 0,1ml =100µg morphine/300ml saline

- Group KT: 0,1 ml saline/300 ml naropin 0.2% ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02264821
Study type Interventional
Source Brugmann University Hospital
Contact
Status Completed
Phase Phase 3
Start date February 2012
Completion date August 2014