Comparing pain relief methods after neck surgery
Comparison of the Postoperative Analgesic Efficacy of Serratus Posterior Superior Intercostal Plane Block and Erector Spinae Plane Block in Anterior Cervical Discectomy
This study tests two different ways to block pain after neck surgery to see which one helps patients feel better and need fewer painkillers.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 85 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Ankara Etlik City Hospital Government |
| Locations | 1 site (Altındağ, Ankara) |
| Trial ID | NCT06639022 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two different nerve block techniques, the serratus posterior superior intercostal plane block and the erector spinae plane block, in managing postoperative pain for patients undergoing anterior cervical discectomy. By comparing these methods to a control group that does not receive a nerve block, the study seeks to determine which technique provides better analgesic outcomes and reduces the need for opioids. The goal is to enhance pain management while minimizing potential side effects associated with opioid use.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-80 with a moderate health status and a BMI between 18-30.
Not a fit: Patients with severe health conditions, those under 18 or over 80 years old, or with a BMI outside the specified range may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing neck surgery, reducing reliance on opioids.
How similar studies have performed: Previous studies have shown promising results with similar nerve block techniques in postoperative pain management, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18-80 years * American Society of Anesthesiologists (ASA) score I-II-III * Body Mass Index (BMI) between 18-30 kg/m2 Exclusion Criteria: * Patients under 18 and over 80 years of age * ASA score IV and above * Patients with a history of bleeding diathesis * BMI below 18 or above 30 kg/m2
Where this trial is running
Altındağ, Ankara
- Ankara Etlik City Hospital — Altındağ, Ankara, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Atakan Sezgi
- Email: kansezgi@gmail.com
- Phone: 00905323327000
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.