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Clinical Trials/NCT06700746
NCT06700746
Completed
Not Applicable

Efficacy of Dextrose Prolotherapy Compare With Extracorporeal Shock Wave Therapy in the Treatment of Chronic Rotator Cuff Tendinopathy

Mahidol University1 site in 1 country24 target enrollmentStarted: November 10, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Songsuda Roongsaiwatana

Principal Investigator

Mahidol University

Study Sites (1)

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