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Clinical Trials/NCT01160913
NCT01160913
Completed
Phase 3

Evaluation of Optimal Anatomical Layer for Continuous Wound Infusion of Local Anesthetics Combined With NSAIDs Through a Multiorifice Catheter for Postoperative Pain Intensity After Elective Cesarean Delivery

Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation1 site in 1 country56 target enrollmentOctober 2007
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ConditionsCesarean Section

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Cesarean Section
Sponsor
Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation
Enrollment
56
Locations
1
Primary Endpoint
Cumulative intravenous morphine consumption
Status
Completed
Last Updated
15 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this randomized double-blind study is to evaluate in which anatomical layer (AF versus BF) continuous wound infusion of local anesthetics combined with NSAIDs through a multiorifice catheter has the best effectiveness during the first 48 hours on postoperative pain intensity after elective cesarean delivery.

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
December 2008
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation

Eligibility Criteria

Inclusion Criteria

  • •elective Cesarean Section under spinal anesthesia over37 weeks' gestation

Exclusion Criteria

  • •allergy to NSAIDs
  • •ASA III or higher
  • •refusal to participate

Outcomes

Primary Outcomes

Cumulative intravenous morphine consumption

Time Frame: 48 hours

Secondary Outcomes

  • Postoperative pain intensity at rest and mobilization(admission, 3,6,12,24,36,48h)
  • adverse effects (nausea, vomiting, itching, sedation)

Study Sites (1)

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