Status:
COMPLETED
Effects of Dextrose Prolotherapy in Rotator Cuff Disease
Lead Sponsor:
Istanbul University
Conditions:
Rotator Cuff Disease
Eligibility:
All Genders
30-65 years
Phase:
NA
Brief Summary
The aim of this prospective, randomized, controlled, single-blind study is to determine the effects of dextrose prolotherapy on shoulder pain and functions in patients with chronic rotator cuff diseas...
Detailed Description
Rotator cuff disease is a major cause of shoulder pain and disability. Non-surgical treatments to reduce pain and improve function have included therapeutic exercises, NSAIDs, subacromial corticostero...
Eligibility Criteria
Inclusion
- Shoulder pain for more than 3 months
- Being resistant to conservative treatment for at least 3 months
- Being in the age range of 30-65
- Presence of rotator cuff disease detected in current magnetic resonance imaging and confirmed by clinical examination.
Exclusion
- Presence of rheumatic disease or other systemic inflammatory diseases
- Having a diagnosis of uncontrolled diabetes mellitus
- Evidence of infection (systemically or locally on the shoulder)
- The presence of a previous operation on the shoulder
- Bleeding tendency (acquired or hereditary) \[INR\> 2 in the patient using coumadin\]
- Injected shoulder within the previous 8 weeks
- The presence of local anesthesia and corn allergy
- Passive shoulder abduction \<100 ° or external rotation \<25 °
- Rotator cuff calcification diameter\> 0.8cm in current direct graph or Usg
- Presence of serious comorbidity
Key Trial Info
Start Date :
March 18 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 12 2021
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04805242
Start Date
March 18 2021
End Date
November 12 2021
Last Update
July 12 2024
Active Locations (1)
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1
Istanbul University Istanbul Faculty of Medicine, Department of Physical Medicine and Rehabilitation
Istanbul, Fatih, Turkey (Türkiye), 34034