Status:
RECRUITING
Erector Spinae Plane Block in Lumbar Spinal Fusion
Lead Sponsor:
Clinique Saint Jean, France
Conditions:
Lumbar Spinal Fusion
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this study is to observe or not a reduction in the consumption of morphine within 72 hours of the realization of an erector spinae plane block when preparing for a lumbar spinal fusion.
Detailed Description
Posterior lumbar spine surgery is surgery described by patients as painful. For this type of surgery, lumbar spinal fusion, especially because of greater exposure, is more painful than simple surgerie...
Eligibility Criteria
Inclusion
- Patient with medical insurance.
- Patient who received information about study and signes a consent to participate in the study.
- Major patient requiring a lumbar spinal fusion surgery.
- Patient with an ASA score of 1, 2 or 3.
Exclusion
- Minor patient.
- Patient with morphine intolerance
- Patient with allergy to local anesthetics.
- Patient consuming morphine for more than 3 months.
- Pregnant or breastfeeding patient.
- Patient scheduled for cancer surgery or trauma surgery.
- Patient participating in another interventional study.
- Patient with history of lumbar spinal fusion.
- Patient requiring lumbar surgery without arthrodesis.
- Patient requiring lumbar surgery with inter-lamar or inter-epineal stabilization.
- Patient refusing to sign the consent form.
- Patient for whom it is impossible to give informed information.
- Patient under the protection of justice, under curatorship or under tutorship.
Key Trial Info
Start Date :
January 3 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
130 Patients enrolled
Trial Details
Trial ID
NCT04904575
Start Date
January 3 2022
End Date
December 31 2026
Last Update
November 24 2025
Active Locations (1)
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1
Clinique Saint Jean
Saint-Jean-de-Védas, France, 34430