Erector Spinae Plane Block in Lumbar Spinal Fusion : Double-blind, Randomized Controlled Trial.
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
France
Clinique Saint Jean
RECRUITING
Saint-jean-de-védas
Contact Information
Primary
Julie SOULIER
julie.soulier@capsante.fr
04 67 61 20 71
Time Frame
Start Date: 2022-01-03
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 130
Treatments
Experimental: Block
The Block group will be made up of patients who will benefit from an injection of levobupivacaine for the realization of the erector spinae plane block.
Placebo_comparator: Placebo
The placebo group corresponds to the reference group, that is to say that it will consist of patients who will benefit from an injection of physiological serum for the realization of the erector spinae plane block.
Related Therapeutic Areas
Sponsors
Leads: Clinique Saint Jean, France