Effect of Ultrasound-guided Hyaluronic or Corticosteroid Injections in Patients With Chronic Subacromial Bursitis
CompletedNot applicableNCT02702206
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
A randomized controlled trial to compare the effect of ultrasound-guided hyaluronic or corticosteroid injections in patients with chronic subacromial bursitis.
Study details
- Official title
- Effect of Ultrasound-guided Hyaluronic or Corticosteroid Injections in Patients With Chronic Subacromial Bursitis
- Conditions
- Shoulder Pain
- Subdeltoid Bursitis
- Subacromial Bursitis
- Interventions
- Drug: corticosteroids
- Drug: hyaluronic acid
- Drug: normal saline
- Sponsor
- Shin Kong Wu Ho-Su Memorial Hospital
- Collaborators
- Ministry of Science and Technology, Taiwan
- Start date
- 2014-08
- Primary completion
- 2016-10
- Sex
- All
- Age range
- from 20 Years
- Results posted
- No results posted in this snapshot
- Countries
- Taiwan
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. shoulder pain for more than 1 month 2. age ≥ 20 years old 3. painful abduction or internal rotation with a visual analog scale (VAS) pain score ≥4 4. the presence of a painful arc of motion or pain at the middle to terminal range of shoulder abduction or internal rotation with a soft end feel 5. tenderness over the subacromial bursa 6. a reduction in pain of ≥40% on active shoulder abduction or internal rotation at the terminal range after injection of 3ml of 1%lidocain into the SASD bursa under ultrasound (US) guidance. Exclusion Criteria: 1. a history of uncontrolled chronic diseases, e.g., malignant neoplasms, blood dyscrasia, and infection 2. previous surgery of the affected shoulder 3. any evidence of a rotator cuff tear or tendinopathy, demonstrated by positive resistive tests or sonographic findings 4. calcification of the rotator cuff, demonstrated by x-ray or sonographic findings 5. the presence of arthritis, such as inflammatory arthritis (e.g., rheumatoid arthritis, seronegative spondyloarthropathy, or crystal-related arthropathy), osteoarthritis, frozen shoulder, subacromial spurs, or deformity of the acromion 6. the presence of instability of the affected shoulder 7. a previous fracture near the shoulder region 8. the presence of cervical radiculopathy or myelopathy 9. having received a corticosteroid or hyaluronic acid subacromial or shoulder joint injection in the past 3 months
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02702206