Comparing different doses of lidocaine during lumbar spinal surgery
Comparison of the Effect of Lidocaine Infusion Applied at Different Doses During Lumbar Spinal Surgery on Hemodynamics and Postoperative Pain
This study is testing whether giving different doses of lidocaine during lumbar spine surgery can help reduce pain and improve recovery for patients afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Ankara University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT05936190 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of intravenous lidocaine infusion at two different doses (1 mg/kg/h vs. 2 mg/kg/h) during lumbar stabilization surgery. The primary focus is on assessing postoperative pain levels, opioid use, and hemodynamic stability in patients. By analyzing the impact of lidocaine on pain management and cardiovascular responses, the study aims to enhance recovery and neurological evaluation post-surgery. The research builds on previous findings that suggest lidocaine can reduce sympathetic reflex responses and improve postoperative outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients classified as ASA 1 or 2 undergoing lumbar stabilization surgery.
Not a fit: Patients classified as ASA 3, 4, or 5, as well as pediatric patients, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and reduced opioid use in patients undergoing lumbar spinal surgery.
How similar studies have performed: Previous studies have shown positive outcomes with lidocaine infusion in various surgical procedures, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ASA 1,2 Exclusion Criteria: * ASA 3,4,5 * Pediatric Patients
Where this trial is running
Ankara
- Ankara University — Ankara, Turkey (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.