Comparison of Spinoglenoid and Suprascapular Notch Approaches and Neuromodulation of the Suprascapular Nerve Under Ultrasonography Guided in Shoulder Pain
pain
1 other identifier
observational
100
1 country
1
Brief Summary
Shoulder pain is a musculoskeletal system (MSS) disease that is frequently seen in adults and tends to become chronic. It ranks 3rd among MSS diseases after low back and knee pain. The main causes of shoulder pain are compression syndromes, acromioclavicular (AC) and glenohumeral joint degeneration, adhesive capsulitis, and biceps tendinopathy. Pathology may be in the joint, bone, muscle, tendon ligament, or bursa. Pain restricts the passive and active range of motion of the shoulder joint, impairing the quality of daily life and activity. It is thought to be between 20% and 50% in the adult population in a 1-year period, and its lifetime prevalence is approximately 10%. Central sensitization develops in cases where the pain is progressive and becomes chronic over time. It has been observed that it becomes chronic in more than 40% of patients in a 1-year period. Thus, shoulder pain becomes a biopsychosocial disease over time. Physical therapy, medical, interventional methods, and surgery are applied in the treatment of shoulder pain. In physical therapy, exercises and some physical medicine modalities are applied to increase joint range of motion and reduce pain, while in medical treatment, oral analgesics, myorelaxants, and topical analgesics are used. Interventional intra-articular steroid injections and distal suprascapular nerve (SS) blockade radiofrequency applications are among the effective treatment options.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedFirst Submitted
Initial submission to the registry
February 22, 2025
CompletedFirst Posted
Study publicly available on registry
February 28, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2025
CompletedSeptember 19, 2025
September 1, 2025
4 months
February 22, 2025
September 17, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Activity visual analogue scale (VAS)
one year
Study Arms (1)
Comparison of Spinoglenoid and Suprascapular Notch Approaches and Neuromodulation of the Suprascapul
Comparison of Spinoglenoid and Suprascapular Notch Approaches and Neuromodulation of the Suprascapular Nerve under Ultrasonography Guided in Shoulder Pain
Eligibility Criteria
\- Patients over the age of 18 who have pain at or above visual analog scale (VAS) 4 despite pharmacological agents and physical therapy (passive range of motion, strengthening exercises) for more than 3 months and who meet the inclusion criteria will be included in the study.
You may qualify if:
- Patients with complete data to be scanned in their files
You may not qualify if:
- Patients with known malignancy,
- patients who had shoulder injections within the last 3 months,
- patients who changed their medical analgesic treatment or underwent surgery during follow-up,
- patients with previous shoulder surgery or deformity,
- patients with inflammatory arthritis and fibromyalgia,
- patients with known cervical disc herniation,
- patients with pacemakers, pregnant women,
- patients with chronic decompensated disease,
- hemiplegic patients,
- patients with major psychopathology,
- patients allergic to medications used during the procedure,
- patients with infection in the procedure area,
- patients with bleeding disorders, and patients who did not agree to participate in the study were excluded from the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kanuni Sultan Süleyman Training and Research Hospital
Istanbul, Turkey, 34000, Turkey (Türkiye)
Study Officials
- STUDY DIRECTOR
altun
Kanuni Sultan Süleyman Training and Research Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- pain specialist
Study Record Dates
First Submitted
February 22, 2025
First Posted
February 28, 2025
Study Start
January 1, 2025
Primary Completion
May 1, 2025
Study Completion
June 1, 2025
Last Updated
September 19, 2025
Record last verified: 2025-09