Image

Evaluation Of Three Different Anagesic Techniques In Patients Undergoing Lumbar Fixation Surgery

Evaluation Of Three Different Anagesic Techniques In Patients Undergoing Lumbar Fixation Surgery

Recruiting
18-65 years
All
Phase N/A

Powered by AI

Overview

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.

Eligibility

Inclusion Criteria:

  • Patients scheduled to undergo lumbar fixation surgery under general anesthesia
  • aged between 18 and 65 years,
  • American Society of Anesthesiologists physical status classification of I-II

Exclusion Criteria:

  • Patients with a known allergy to local anesthetics.
  • Patients who used opioid analgesics within 48 hours prior to sample collection.
  • Patients with a history of smoking or alcohol consumption.
  • Patients with conditions affecting salivary flow, such as xerostomia or those who have undergone radiotherapy.
  • Patients with infectious diseases known to be transmissible through saliva.
  • Patients with an ASA physical status classification of III or higher.
  • Patients unable to use a patient-controlled analgesia (PCA) device.
  • Patients who do not consent to the study procedures.

Study details
    Lumbar Fixation Surgery

NCT06801574

Ataturk University

15 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.