Erector Spinae Plane Block in Lumbar Spinal Fusion
- Conditions
- Lumbar Spinal Fusion
- Registration Number
- NCT04904575
- Lead Sponsor
- Clinique Saint Jean, France
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria:<br><br> - Patient with medical insurance.<br><br> - Patient who received information about study and signes a consent to participate in<br> the study.<br><br> - Major patient requiring a lumbar spinal fusion surgery.<br><br> - Patient with an ASA score of 1, 2 or 3.<br><br>Exclusion Criteria:<br><br> - Minor patient.<br><br> - Patient with morphine intolerance<br><br> - Patient with allergy to local anesthetics.<br><br> - Patient consuming morphine for more than 3 months.<br><br> - Pregnant or breastfeeding patient.<br><br> - Patient scheduled for cancer surgery or trauma surgery.<br><br> - Patient participating in another interventional study.<br><br> - Patient with history of lumbar spinal fusion.<br><br> - Patient requiring lumbar surgery without arthrodesis.<br><br> - Patient requiring lumbar surgery with inter-lamar or inter-epineal stabilization.<br><br> - Patient refusing to sign the consent form.<br><br> - Patient for whom it is impossible to give informed information.<br><br> - Patient under the protection of justice, under curatorship or under tutorship.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Consumption of postoperative morphine within 72 hours of the operation.
- Secondary Outcome Measures
Name Time Method Digital visual scale to assess pain of patient within 72 hours of the operation.;Onset of nausea and vomiting within 72 hours of the operation.;Onset of complication within 30 days of the intervention.;Walking perimeter measurement by the physiotherapist during the 72 hours following the intervention.