The Tap Block Technique Via the Anterior Approach in Elective Surgery of the Spine
Phase 4
Completed
- Conditions
- Elective Surgery of the Spine by Laparotomy
- Interventions
- Drug: Chlorure de sodium 0.9%
- Registration Number
- NCT02055664
- Lead Sponsor
- Centre Hospitalier Universitaire Dijon
- Brief Summary
This is a prospective, single-centre, randomised, double-blind trial, comparing TAP block with continuous infiltration of ropivacaine versus placebo.
Procedure:
Once consent has been obtained, patients will be randomised into one of the two groups: Ropivacaine or Placebo. At the end of the operation, the TAP block will be implemented via a catheter inserted by the anaesthetist.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
- Patients over 18 yo who have provided written informed consent
- Patients with an indication for elective spinal surgery using laparotomy
- Patients with national health insurance cover
Exclusion Criteria
- Adults under guardianship
- Pregnant or breast-feeding women
- allergies or contra-indication for paracetamol, morphine-based drugs
- Contra-indication for ropivacaine
- Contra-indication for sodium chloride
- inability to understand PCA (patient-controlled anaesthesia)
- Hypersensitivity to ropivacaine or to other aminoamide local anaesthetics
- Hypovolemia
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description treatment Chlorure de sodium 0.9% - control Ropivacaine 0.2% -
- Primary Outcome Measures
Name Time Method Consumption of morphine in mg First 48 hours following the surgery
- Secondary Outcome Measures
Name Time Method Intensity of pain First 48 hours following the surgery
Trial Locations
- Locations (1)
CHU de Dijon
🇫🇷Dijon, France