Erector Spinae Plane Block in Lumbar Release Surgery (NCT04925882) | Clinical Trial Compass
CompletedNot Applicable
Erector Spinae Plane Block in Lumbar Release Surgery
France100 participantsStarted 2022-01-03
Plain-language 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 non-instrumented spine surgery.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patient with medical insurance.
* Patient twho received information about study and signes a consent to participate in the study.
* Major patient to be operated on for lumbar release surgery without arthrodesis or osteosynthesis posterior (herniated disc repair, one or two level recalibration, laminectomy) +/- implant interlaminar.
* Patient with an ASA score of 1, 2 or 3.
Exclusion Criteria:
* 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 a history of lumbar arthrodesis.
* Patient requiring lumbar surgery with arthrodesis.
* 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.
What they're measuring
1
Consumption of postoperative morphine within 72 hours of the operation