NCT06700746
Completed
Not Applicable
Efficacy of Dextrose Prolotherapy Compare With Extracorporeal Shock Wave Therapy in the Treatment of Chronic Rotator Cuff Tendinopathy
ConditionsChronic Rotator Cuff Tendinopathy
Overview
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Mahidol University
- Enrollment
- 24
- Locations
- 1
- Primary Endpoint
- VAS score
Overview
Brief Summary
To compare the efficacy of dextrose solution injection with ESWT for pain reduction in rotator cuff tendinopathy.
Additionally, secondary objective is to evaluate DASH and active range of motion of shoulder joint
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Investigator)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Chronic shoulder pain for at least 3 months
- •Unilateral affected side
- •History of unsuccessful conservative treatment
- •Age 18 years or older
Exclusion Criteria
- •Rotator cuff complete tear
- •Local or generalized arthritis
- •Previous shoulder surgery
- •Previous history allergy to local anesthesia
- •Pregnancy
- •Current infectious or tumorous disease
- •Dysfunction in the neck or thoracic region of both
- •Coagulation disturbance
Outcomes
Primary Outcomes
VAS score
Time Frame: Assessment at baseline, three weeks, six weeks, three months and six months after the end of the treatment
Pain reduction VAS
Secondary Outcomes
- Function DASH score(Assessment at baseline, three weeks, six weeks, three months and six months after the end of the treatment)
- Shoulder ROM(Assessment at baseline, three weeks, six weeks, three months and six months after the end of the treatment)
Investigators
Songsuda Roongsaiwatana
Principal Investigator
Mahidol University
Study Sites (1)
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