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 range

18 Years

Sex

ALL

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.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Consumption of postoperative morphine within 72 hours of the operation

Timeframe: 72 hours

Trial details

NCT IDNCT04925882

SponsorClinique Saint Jean, France

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-19

View on ClinicalTrials.gov More Hernia Lumbar trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.