Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
227 participants
OBSERVATIONAL
2023-09-13
2023-11-01
Brief Summary
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Detailed Description
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The demographic characteristics of the patients were recorded.
First of all, common extensor tendon tears, if it existed, were demonstrated with ultrasonography. Then, primary and secondary outcome measures were performed.
Maximum tendon thickness measurements (capitellar - radiocapitellar) and the presence of bone abnormality were detected with ultrasonography of the lateral epicondyle region of the humerus.
The VAS was used to assess pain and was evaluated separately for pain at rest (VAS-rest), at night (VAS-night), and during ADL (VAS-ADL).
Force was applied on the lateral epicondyle using a standard pressure algometer (Baseline®) to evaluate the patient's sensitivity to pain. The pressure at which the patient first felt pain and the average value in kg/cm2 (repeated three times) were recorded.
PRTEE consists of two sub-sections (pain and function): the severity of pain in the elbow and functional deficiencies. The Turkish version of the PRTEE questionnaire was used
The hand dynamometer (JAMAR®) was used to assess the hand grip strength. The patient was positioned with sitting, shoulder adduction, elbow 90° flexion, and forearm in a position between supination and pronation. The average value in kilogram-force (repeated three times). Between repeated measures 1-minute resting, periods were given.
Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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with common extensor tendon tears
the participants who have common extensor tendon tears demonstrated with ultrasonography.
No interventions assigned to this group
without common extensor tendon tears
the participants who do not have common extensor tendon tears demonstrated with ultrasonography.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* diagnosis of LE based on clinical parameters and US findings
* duration of symptoms ranging from 2 to 12 weeks
* agreement to participate in the study
Exclusion Criteria
* has received any treatment for lateral epicondylitis before
* previous elbow surgery
* history of elbow fracture
* upper extremity muscle weakness due to radiculopathy or neuropathy
* the presence of concurrent neurological, rheumatic, psychiatric, or malignant conditions
* pregnancy
* inability to comply with the study requirements
18 Years
65 Years
ALL
No
Sponsors
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Dokuz Eylul University
OTHER
Responsible Party
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Banu Dilek
Assoc Prof
Principal Investigators
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Banu Dilek, Assoc Prof
Role: STUDY_CHAIR
Dokuz Eylul University
Locations
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Dokuz Eylul University
Izmir, , Turkey (Türkiye)
Countries
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Other Identifiers
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LEtendontears
Identifier Type: -
Identifier Source: org_study_id
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