Erector Spinae Plane Block in Lumbar Spinal Fusion

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Lumbar Spinal Fusion

In brief

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.

Key facts

Study ID

NCT04904575

Run by

Clinique Saint Jean, France

People needed

130

Starts

2022-01-03

Expected to finish

2026-12-31

Last updated by the study team

2025-11-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 may not qualify if…

• 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.

Where it is running

• Clinique Saint Jean — Saint-Jean-de-Védas, France (enrolling)

Full record on ClinicalTrials.gov

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