Conservative Treatment in Lateral Epicondylitis

NCT ID: NCT06730789

Last Updated: 2024-12-12

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

Clinical Phase

NA

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-15

Study Completion Date

2022-05-15

Brief Summary

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Conservative treatments follow the vast majority of treatments in lateral epicondylitis. In this research, we aimed to elucidate the treatment outcomes of patients via epicondylitis bandage, wrist dorsiflexion splint, and kinesio tape groups by sequential randomization and to compare treatment outcomes.

Detailed Description

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Conditions

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Lateral Epicondylitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Lateral Epicondylitis (treatment with epicondylitis bandage)

Patients with diagnosis of lateral epicondylitis.

Group Type EXPERIMENTAL

Epicondylitis bandage

Intervention Type DEVICE

A conservative treatment method of lateral epicondylitis.

Lateral Epicondylitis (treatment with wrist dorsiflexion orthesis)

Patients with diagnosis of lateral epicondylitis.

Group Type EXPERIMENTAL

Wrist dorsiflexion splint

Intervention Type DEVICE

A conservative treatment method of lateral epicondylitis.

Lateral Epicondylitis (treatment with kinesio tape)

Patients with diagnosis of lateral epicondylitis.

Group Type EXPERIMENTAL

Kinesio tape

Intervention Type DEVICE

A conservative treatment method of lateral epicondylitis

Interventions

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Epicondylitis bandage

A conservative treatment method of lateral epicondylitis.

Intervention Type DEVICE

Wrist dorsiflexion splint

A conservative treatment method of lateral epicondylitis.

Intervention Type DEVICE

Kinesio tape

A conservative treatment method of lateral epicondylitis

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients who were ≥18 years of age, and had no history of elbow surgery.
* Participants should have pain and sensitivity, with symptom duration less than 12 weeks.
* Patients with a positive result in one of the provocation tests (Maudsley's Test-resisted middle finger extension extensor carpi radialis test), resisted wrist extension, or passive stretching of the wrist extensors (Mill's Test) were included.

Exclusion Criteria

* Patients under 18 years of age,
* patients who did not consent to participate in the study,
* those who had previous surgery on the elbow,
* presence of cervical spondylosis and radiculopathy,
* presence of endocrine disease,
* presence of autoimmune disease,
* presence of concomitant entrapment neuropathy or polyneuropathy,
* pregnancy,
* presence of systemic inflammatory disease,
* presence of acute trauma,
* presence of deformity in the upper extremity,
* presence of metabolic disease,
* presence of elbow arthritis,
* presence of allergy to kinesio tape and orthoses,
* having received treatment for lateral epicondylitis in the past (exercise, injection, NSAIDs).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Uludag University

OTHER

Sponsor Role lead

Responsible Party

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Yücel Bilgin

MD, Orthopedics and Traumatolody Specialist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Bursa Uludag University

Bursa, Nilüfer, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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IEAH-YB-2020-01

Identifier Type: -

Identifier Source: org_study_id