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Study identifier: NCT06801574 Synced from ClinicalTrials.gov · July 28, 2026
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Evaluation Of Three Different Anagesic Techniques In Patients Undergoing Lumbar Fixation Surgery

Condition: Lumbar Fixation Surgery  ·  Sponsor: Ataturk University

PhaseNA
Planned participants84
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Lumbar spinal stenosis is a degenerative condition characterized by the narrowing of the space surrounding the neurovascular structures of the lumbar vertebrae, resulting from age-related changes in the intervertebral discs, ligamentum flavum, and facet joints. It commonly causes unilateral pain in the lower back, hips, and legs, often described as cramping or burning. Postoperative pain management in these cases frequently involves oral opioids or intravenous administration using patient-controlled analgesia devices. However, opioids are associated with side effects such as reduced gastrointestinal motility, urinary retention, and respiratory depression. To mitigate these issues, local anesthetic wound infiltration is widely employed by surgeons to manage postoperative pain and reduce opioid consumption following lumbar spinal surgeries. The primary aim of this study is to compare the postoperative efficacy of three different analgesic methods in patients undergoing elective lumbar fixation surgery, using the percentage change in salivary opiorphin levels as a marker. Additionally, the study seeks to evaluate the correlation between these changes and postoperative pain scores, as well as the amount of opioids consumed.

This description comes directly from the study's public registry record.

Talk to the study team

Feyza Simsek  ·  +90 554 947 52 61  ·  feyzasimsek0205@gmail.com

Canan Atalay  ·  +90 (533) 363 53 18

Always discuss trial participation with your own doctor first.

Locations (1)

Ataturk UniversityErzurum, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT06801574