Status:
UNKNOWN
Continuous Pre-uterine Wound Infiltration Versus Intrathecal Morphine for Postoperative Analgesia After Cesarean Section
Lead Sponsor:
Central Hospital, Nancy, France
Collaborating Sponsors:
Maternite Regionale Universitaire
Conditions:
Postoperative Pain
Eligibility:
FEMALE
18-55 years
Phase:
PHASE4
Brief Summary
The cesarean section is considered as a painful surgery during the post operative period. Mothers may need to move immediately after the surgery to take care of their babies. This may increase the ris...
Detailed Description
The aim of this study is to compare the efficacy of continuous wound infiltration versus intrathecal morphine for postoperative analgesia after scheduled cesarean section. The primary endpoint is morp...
Eligibility Criteria
Inclusion
- Elective Cesarean section
- Spinal anesthesia
- Singleton
- ASA ( Physical status score) 1 to 3
Exclusion
- Age \<18yrs
- BMI ≥ 45 kg/m2 or weight \< 45 kg
- Refusal to consent
- Urgent cesarean section
- Allergy to a medication used in the protocol
- Impaired hemostasis ou current infection
- Contra indication or failure of spinal anesthesia
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2017
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT02279628
Start Date
July 1 2014
End Date
June 1 2017
Last Update
October 31 2014
Active Locations (1)
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1
Maternité Régionale Universitaire (MRU)
Nancy, Lorraine, France, 54000