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Clinical Trials/NL-OMON20120
NL-OMON20120
Not yet recruiting
Not Applicable

Effectiveness of Ultrasound Guided Percutaneous treatment of Lateral Epicondylitis using standardized perforation with application of autologous blood, dextrose or perforation only, in relation to pain and functional recovery; A randomized controlled trial

Amphia hospital Breda. OLVG Amsterdam. AMC Amsterdam0 sites165 target enrollmentTBD
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Conditionslateral epicondylitis, treatment, injectables, RCT.

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
lateral epicondylitis, treatment, injectables, RCT.
Sponsor
Amphia hospital Breda. OLVG Amsterdam. AMC Amsterdam
Enrollment
165
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Amphia hospital Breda. OLVG Amsterdam. AMC Amsterdam

Eligibility Criteria

Inclusion Criteria

  • •Patients referred by their GP to the orthopaedic surgeon diagnosed with unilateral Lateral Epicondylitis lasting longer than 6 weeks
  • •Age between 18 and 65 years

Exclusion Criteria

  • •A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • •Prior injection therapy (during this episode of LE), surgery or trauma at the affected elbow.

Outcomes

Primary Outcomes

Not specified

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