Optimal Site of Administration for Continuous Wound Infusion After Cesarean Section

Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation56 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Cesarean Section

Interventions

Continuous wound infusionPROCEDURE

Continuous woundPROCEDURE

Eligibility

Sex: FEMALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * elective Cesarean Section under spinal anesthesia over37 weeks' gestation Exclusion Criteria: * allergy to NSAIDs * ASA III or higher * refusal to participate

Locations (1)

Hôpital Cochin

Paris, France

Outcomes

Primary Outcomes

Cumulative intravenous morphine consumption

Time frame: 48 hours

Secondary Outcomes

Postoperative pain intensity at rest and mobilization

Time frame: admission, 3,6,12,24,36,48h

adverse effects (nausea, vomiting, itching, sedation)

Data from ClinicalTrials.gov

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