Echo-guided Transverse Abdominal Plane Block (TAP) in Anterior Lumbar Arthrodesis (ALIF)

• Status: Recruiting
• Trial end date: 2025-07-01
• Target enrollment: 0
• Participant gender: All

Summary

The goal of this interventional study is to is to compare the effect of a tap block versus a placebo in patients undergoing anterior lumbar spine surgery.

The main question it aims to answer :

• whether tap block can reduce the need for postoperative pain medication Participants will be randomized into two groups and all postoperative pain medication will be recorded over 3 days.

Researchers will compare tap block vs placebo to see if it reduces postoperative pain.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Clinique Saint Jean, France
• Treatments: Levobupivacaine

Criteria

Inclusion Criteria:

Patient affiliated or entitled to a social security plan.

• Patient who has been informed about the study and has co-signed a consent form with the investigator. consent to participate in the study.

• Patients over 18 years of age scheduled for abdominal disc surgery on one or two levels.

• Patient with ASA criteria 1, 2 and 3.

Exclusion Criteria:

• Patients with intolerance or contraindication to paracetamol, anti-inflammatory or morphine.

• Patients allergic to local anesthetics.

• Pregnant or breast-feeding patient.

• patient undergoing cancer or trauma surgery trauma.

• Patient participating in another interventional study.

• Patient with a history of lumbar arthrodesis.

• Patient refusing to sign consent form.

• Patient unable to give informed consent.

• Patient under court protection, guardianship or trusteeship.

• Patient not available for study follow-up.