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Search / Trial NCT04904575

Erector Spinae Plane Block in Lumbar Spinal Fusion

Launched by CLINIQUE SAINT JEAN, FRANCE · May 26, 2021

Trial Information

Current as of July 09, 2025

Recruiting

Keywords

Erector Spinae Plane Block Consumption Of Morphine

ClinConnect Summary

This clinical trial is looking at a pain management technique called the erector spinae plane block to see if it can help reduce the need for morphine in patients undergoing lumbar spinal fusion surgery. The goal is to find out if using this technique before surgery can lead to less morphine use in the first 72 hours after the procedure, which may help improve recovery and comfort for patients.

To participate in this study, you need to be between 65 and 74 years old, have medical insurance, and be scheduled for lumbar spinal fusion surgery. You also need to understand the study and agree to join by signing a consent form. However, if you have certain conditions, like being allergic to local anesthetics, pregnant, or have had prior lumbar surgery, you may not be eligible. If you choose to participate, you'll receive more information about what to expect, including details on the procedure and how your pain management will be handled during your recovery.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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.
  • 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 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.

About Clinique Saint Jean, France

Clinique Saint Jean, located in France, is a leading healthcare institution dedicated to delivering high-quality medical care and advancing clinical research. Renowned for its state-of-the-art facilities and a multidisciplinary team of healthcare professionals, the clinic actively participates in clinical trials aimed at enhancing treatment options and patient outcomes. With a commitment to innovation and patient-centered care, Clinique Saint Jean plays a pivotal role in the investigation of new therapies and medical technologies, contributing to the advancement of healthcare knowledge and practices both locally and globally.

Locations

Saint Jean De Védas, , France

Patients applied

0 patients applied

Trial Officials

Guillaume LONJON, MD

Principal Investigator

Clinique Saint Jean, Saint Jean de Védas

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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