The Effect of Tendon Tears on Lateral Epicondylitis

NCT ID: NCT06206109

Last Updated: 2024-01-18

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

227 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-09-13

Study Completion Date

2023-11-01

Brief Summary

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Common extensor tendon (CET) tears that can be detected with ultrasonography (US) may be associated with worsening clinical and other ultrasonographic parameters in patients with LE. In this retrospective evaluation of patients with lateral epicondylitis (LE), the effect of common extensor tendon (CET) tears revealed by ultrasonography (US) with demographic, clinical, and other US findings was investigated.

Detailed Description

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The files of 227 patients with LE who applied to Dokuz Eylül University Faculty of Medicine, Department of Physical Medicine and Rehabilitation Clinic and met the inclusion and exclusion criteria were reviewed retrospectively.

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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Lateral Epicondylitis Tennis Elbow Tendon Tear

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

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

* age between 18-65 years
* 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

* LE findings in the other extremity
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dokuz Eylul University

OTHER

Sponsor Role lead

Responsible Party

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Banu Dilek

Assoc Prof

Responsibility Role PRINCIPAL_INVESTIGATOR

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)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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LEtendontears

Identifier Type: -

Identifier Source: org_study_id

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