Comparing two types of nerve blocks for pain relief after shoulder surgery
Comparison of the Postoperative Analgesic Efficacy of Serratus Posterior Superior Intercostal Plane Block and Interscalene Brachial Plexus Block in Shoulder Arthroscopy
This study is testing which of two types of nerve blocks can help people aged 18 to 80 feel less pain after shoulder surgery and reduce their need for opioid medications.
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 | NCT06626191 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two different nerve blocks, the interscalene brachial plexus block and the serratus posterior superior intercostal plane block, in managing postoperative pain for patients undergoing shoulder arthroscopy. By comparing these techniques, the study seeks to determine which method provides better analgesia and reduces the need for opioid medications, thereby minimizing potential side effects. The research will involve patients aged 18 to 80 with specific health criteria, and it will assess pain control in the immediate postoperative period.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 80 with a BMI between 18 and 30 and an ASA score of I to III.
Not a fit: Patients under 18 or over 80 years of age, those with a high ASA score, or those 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 shoulder surgery, enhancing recovery and rehabilitation.
How similar studies have performed: Previous studies have shown promising results in pain management using nerve blocks, suggesting that this approach is both effective and beneficial.
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 (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.