Actively Recruiting
Erector Spinae Plane Block in Lumbar Spinal Fusion
Led by Clinique Saint Jean, France · Updated on 2025-11-24
130
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Erector Spinae Plane Block in Lumbar Spinal Fusion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
You will not qualify if you...
- 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.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique Saint Jean
Saint-Jean-de-Védas, France, 34430
Actively Recruiting
Research Team
J
Julie SOULIER
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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