Status:

COMPLETED

Effectiveness of Radial Extracorporeal Shock Wave Therapy and Supervised Exercises in Lateral Epicondylitis

Lead Sponsor:

Istanbul University

Conditions:

Lateral Epicondylitis

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

No consensus has yet been built on the treatment of lateral epicondylitis (LE) due to the lack of evidence. Although conflicting results are present, radial extracorporeal shock wave therapy (rESWT) h...

Detailed Description

ESWT and exercise have beneficial effects on the management of tendinopathies owing to their various mechanisms that showed therapeutic efficacy. Owing to its positive outcomes, extracorporeal shock w...

Eligibility Criteria

Inclusion

  • The diagnosis of LE was made in the clinical examination, and the diagnosis was confirmed with the Southampton Diagnostic Criteria of "the presence of epicondyle pain, and epicondyle pain and tenderness on resisted extension of the wrist.
  • Patients with symptoms lasting longer than 3 months
  • with average pain in the previous week detected as 3 or above on a 10-cm visual analogue scale (VAS)
  • who were aged over 18 years

Exclusion

  • pain in the proximal part of the affected extremity (e.g. shoulder pain, neck pain)
  • abnormal neurogenic symptoms (e.g. radicular pain, numbness) on the affected extremity
  • presence of posterior interosseous nerve entrapment
  • congenital or acquired upper extremity deformities that might affect grip strength
  • systemic musculoskeletal system or neurologic disorders
  • systemic rheumatologic disease or systemic infection
  • presence of malignancy, coagulation disorders, and anticoagulant use
  • inserted cardiac pacemaker
  • history of surgical treatment on the elbow of the affected extremity
  • pregnancy.
  • patients who were administered other treatments such as physical therapy or steroid injections in the last 3 months

Key Trial Info

Start Date :

February 20 2015

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 15 2016

Estimated Enrollment :

41 Patients enrolled

Trial Details

Trial ID

NCT03834090

Start Date

February 20 2015

End Date

January 15 2016

Last Update

February 7 2019

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