Erector Spinae Plane Block in Lumbar Spinal Fusion
ConditionLumbar Spinal Fusion
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorClinique Saint Jean, France
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
Minor patient.
Patient with morphine intolerance
Patient with allergy to local anesthetics.
Patient consuming morphine for more than 3 months.
Trial design
Treatments tested in this trial
- Erector spinae plane block
- Erector spinae plane block
Treatment groups
130 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov