Comparing dexmedetomidine and remifentanil for pain management after spinal surgery
Comparison of the Effects of Remifentanil and Dexmedetomidine on Postoperative Acute Pain in Patients Who Received Erector Spina Plane Block in Spinal Surgeries
This study tests whether using dexmedetomidine or remifentanil during spinal surgery can help patients manage pain better and use fewer opioids afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 74 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Aydin Adnan Menderes University Academic / other |
| Locations | 1 site (Aydın) |
| Trial ID | NCT06264739 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of two different analgesic methods, dexmedetomidine and remifentanil, in patients undergoing erector spinae block for lumbar disc surgery. It is a randomized double-blind study where patients will receive either dexmedetomidine or remifentanil during their surgery, alongside a routine anesthesia protocol. Pain levels will be assessed postoperatively using a Numeric Rating Scale at regular intervals to determine which method provides better pain relief and reduces opioid consumption.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-75 who are scheduled for lumbar disc surgery and have an ASA physical status of 1-3.
Not a fit: Patients who may not benefit from this study include those requiring emergency surgery, those with chronic opioid use, or those with psychiatric disorders.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing spinal surgery, potentially reducing opioid use.
How similar studies have performed: Other studies have shown promising results with similar multimodal analgesia approaches, suggesting potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Written informed consent; * 18-75 years old * ASA Physical Status 1-3; * Patients planned for lumbar disc surgery Exclusion Criteria: * Rejection during registration * Request for dismissal from employment * Inability to give informed consent * Emergency surgery * Bleeding diathesis * Chronic use of opioids * Psychiatric disorders
Where this trial is running
Aydın
- Ferdi Gülaştı — Aydın, Turkey (Recruiting)
Study contacts
- Principal investigator: ferdi gülasştı — Aydin Adnan Menderes University
- Study coordinator: ferdi gülaştı
- Email: ferdigulasti@gmail.com
- Phone: 5054929650
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.