Comparing two types of nerve blocks for shoulder surgery pain relief
Sub Omohyoid Suprascapular Nerve Block Versus Interscalene Nerve Block for Postoperative Shoulder Surgery Pain: Randomized Comparative Study.
This study is testing two different types of nerve blocks to see which one helps reduce pain better after shoulder surgery for patients aged 18 to 60.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Minia University Academic / other |
| Locations | 1 site (Minya) |
| Trial ID | NCT05796778 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of sub omohyoid suprascapular nerve block and interscalene nerve block in managing postoperative pain for patients undergoing shoulder surgery. The goal is to reduce the need for opioids, which can have significant side effects, thereby enhancing recovery in fast track surgical programs. Patients aged 18 to 60 with ASA I-II classifications will be included, while those with certain medical conditions or allergies will be excluded. The study is conducted at Minia University Hospital.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-60 scheduled for shoulder surgery with ASA physical status I or II.
Not a fit: Patients with allergies to local anesthetics, significant obesity, or certain medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for shoulder surgery patients, reducing reliance on opioids.
How similar studies have performed: While nerve blocks are commonly used, the specific comparison of these two techniques in this context is less established, indicating a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Aged 18-60 years. 2. ASA I-II. 3. Both sexes. 4. Shoulder surgery. Exclusion Criteria: 1. Patient refusal 2. Allergy to local anesthetics 3. BMI \>40 kg/m2 4. Bleeding diathesis or history of anticoagulant use. 5. Psychiatric diseases. 6. Infection of the skin at the site of needle punctures area.
Where this trial is running
Minya
- Minia University Hospital — Minya, Egypt (Recruiting)
Study contacts
- Principal investigator: hassan m. hetta, lecturer — Minia University, faculty of medicine
- Study coordinator: hassan m. hetta, lecturer
- Email: hassan.hetta@mu.edu.eg
- Phone: 1010901114
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.