Comparing two types of nerve blocks for pain relief in shoulder surgery
A Randomized Double-blinded Study to Evaluate the Efficacy of PECS II Block Versus Intercostobrachial Ring Block in Patients Undergoing Arthroscopic Rotator Cuff Repair With Open Biceps Tenodesis
This study tests which of two types of nerve blocks can provide better pain relief after shoulder surgery for patients having rotator cuff repair.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 74 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Southern California Academic / other |
| Locations | 1 site (Los Angeles, California) |
| Trial ID | NCT04930393 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two different nerve blocks, the PECS II block and the axillary ring block, in providing postoperative pain relief for patients undergoing rotator cuff repair surgery with biceps tenodesis. The research aims to determine which nerve block offers superior analgesia and reduces intraoperative stimulation. All participants will receive an interscalene block as part of their pain management strategy. The study focuses on medically optimized patients who meet specific eligibility criteria.
Who should consider this trial
Good fit: Ideal candidates are medically optimized patients scheduled for elective arthroscopic rotator cuff repair with open biceps tenodesis.
Not a fit: Patients who are pregnant, breastfeeding, have a history of chronic opioid use, respiratory compromise, or allergies to local anesthetics or opioids 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, reducing reliance on opioids.
How similar studies have performed: Other studies have shown promising results with similar nerve block techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * medically optimized patients who will undergo an elective surgery for an arthroscopic rotator cuff repair with open biceps tenodesis Exclusion Criteria: * women who are pregnant or breastfeeding, history of chronic opioid use, respiratory compromise, smokers, or allergy to local anesthetics or opioids.
Where this trial is running
Los Angeles, California
- Healthcare Center 3 - Keck Hospital of USC — Los Angeles, California, United States (Recruiting)
Study contacts
- Study coordinator: Paul Lee, MD
- Email: pauls.lee@med.usc.edu
- Phone: 4109132126
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.