MedPath

Comparison of two manual techniques in elbow

Not Applicable
Recruiting
Conditions
ateral Epicondylitis.
Lateral epicondylitis, unspecified elbow
M77.10
Registration Number
IRCT20230216057434N1
Lead Sponsor
Self Funded
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
94
Inclusion Criteria

Age: 25- 55 years
Gender: Both gender
Tenderness on palpation over the lateral epicondyle of humerus
Patients has pain for at least 3 month or more duration
Patients with positive cozen test

Exclusion Criteria

Dysfunction in shoulder, neck and thoracic region
Cervical radiculopathy
Corticosteroid injection within 3 months
Patients who had received any conservative treatment in the last 4 weeks before enring in the study.
Recent surgery of elbow joint
Fracture
Soft tissue injury in elbow region

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Assessment will be performed at o week(baseline) and at completion of 4 weeks treatment. Method of measurement: Numeric Pain rating scale.
Secondary Outcome Measures
NameTimeMethod
Range of motion at elbow joint. Timepoint: Assessment will be performed at o week(baseline) and at completion of 4 weeks treatment. Method of measurement: Goniometer.;Functional disability. Timepoint: Assessment will be performed at o week(baseline) and at completion of 4 weeks treatment. Method of measurement: Patient Rated Tennis Elbow Scale(PRTEE).
© Copyright 2025. All Rights Reserved by MedPath