Status:
WITHDRAWN
Post-cesarean Pain Control Via Continuous Infusion of Ropivacain et Diclogenac Into the Wound Versus Intathecal Morphine
Lead Sponsor:
Centre Hospitalier Universitaire de Nīmes
Conditions:
Cesarean Section
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
The goal is to compare the quality of post-cesarean analgesia, the side effects and the incidence of residual scar pain obtained with intrathecal morphine (reference treatment) or with a continuous in...
Eligibility Criteria
Inclusion
- single, normally progressing pregancy
- term \> 36 weeks amenorrhea
- BMI between 20 and 25 kg/m\^2 before pregnancy
- height between 55 and 90 kg
- cesarean section by Joel-Cohen or Pfannenstiel techniques
- patient has signed consent
- patient has social security coverage
Exclusion
- Multiple pregnancy
- pathological pregnancy: hypertension (\>140/90 mmHg found during the pregnancy), pre-eclampsia, gestational diabetes
- term \< 36 weeks amenorrhea
- non-pregnancy related maternal pathology (insufficiency)
- obesity (BMI \> 25 kg/m\^2 before pregnancy)
- height \< 155 cm or \> 180 cm
- weight \< 55 kg or \> 90 kg
- patient refuses to sign consent
- surgical technique other than Joel-Cohen or Pfannenstiel
- hepatic insufficiency (prothrombin \< 60%)
- contra-indications for rachianesthesia: infection, hemostasis problems (platelets \< 80.109/L, prothrombin \< 60%, TCA \> 40s)
- allergy to local anesthestics
- patient is participating in another study, or has participated in another study within the last 6 months
- patient is under any type of guardianship
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01211431
Start Date
September 1 2010
End Date
October 1 2012
Last Update
March 25 2015
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