N/A
N=80
Comparison of the Efficacy of Two Different Suprascapular Nerve Block Techniques in Patients With Chronic Shoulder Pain
Chronic Shoulder Pain
Bottom Line
View on ClinicalTrials.gov: NCT04938037 ↗Enrolled (actual)
80
Serious AEs
0.0%
Results posted
May 2025
Primary outcome: Primary: Change of Shoulder Pain and Disability Index (SPADI) — 22.1; 25.9; 27.0; 36.6 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- US guided, SSNB with 1ml methylprednisolone acetate (1ml / 40mg) and 5 ml 0.5% bupivacaine (Procedure)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- TC Erciyes University
- Primary completion
- Aug 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change of Shoulder Pain and Disability Index (SPADI) |
22.1; 25.9; 27.0; 36.6; 29.4; 34.1 | — |
| SECONDARY Change of Visual Analog Scale (VAS) |
2.2; 2.8; 2.8; 3.7; 2.9; 3.5 | — |
| SECONDARY Change of Range of Motion (ROM) |
-3.9; -9.6; -8.6; -18.6; -8.8; -20.5 | — |
| SECONDARY Change of Pain Pressure Threshold (PPT) |
-0.3; 0.0; -0.1; -0.4; -0.2; -0.3 | — |
| SECONDARY Patient Satisfaction |
3; 2; 8; 1; 3; 6 | — |
Summary
The aim of this study is to compare the efficacy and safety of the suprascapular nerve block (SSNB) at the spinoglenoid notch with SSNB at the suprascapular notch, which is the most commonly used technique in patients with chronic shoulder pain.
Eligibility Criteria
Inclusion Criteria
- Age ≥ 18 years old
- Shoulder pain that last more than 3 month
- Patients with a VAS value of ≥ 4 despite treatment (drugs used for analgesia, local injections and physiotherapy methods)
- Shoulder pain defined as non-specific shoulder pain, subacromial impingement syndrome, rotator cuff tendinopathy, adhesive capsulitis, non-traumatic instability, SLAP lesion, acromioclavicular pathology, and / or shoulder osteoarthritis.
Exclusion Criteria
- A history of uncontrolled chronic diseases, e.g., malignant neoplasms, blood dyscrasia, and infection
- Previous surgery history at the affected shoulder
- Shoulder injection in the last 3 months before treatment
- The presence of cervical radiculopathy or myelopathy
- A previous fracture close to the shoulder region
- Presence of septic arthritis or local infection in the affected shoulder
- Presence of anaphylaxis against local anesthetics and / or corticosteroids
- Presence of a cardiac pacemaker
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT04938037). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.