Recruiting

Ultrasound Response to SNAG in Chronic Medial Epicondylitis Treatment

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What is being tested

SNAG ( sustained natural apopheseal glide )

Other
Who is being recruted

Elbow Tendinopathy+5

+ Elbow Injuries

+ Arm Injuries

From 35 to 50 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: September 2025
See protocol details

Summary

Principal SponsorBeni-Suef University
Study ContactSahar M Abdelmutilibe, PHD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 8, 2025

Actual date on which the first participant was enrolled.

This study focuses on finding new ways to treat medial epicondylitis, also known as golfer's elbow, which causes pain on the inside of the elbow, especially during certain movements like bending the wrist. This condition can lead to difficulties in performing everyday tasks and work-related activities due to pain and other functional issues. Researchers aim to explore whether certain treatments applied to the neck and upper back can improve the condition of the tendons in individuals with this elbow pain. By understanding these effects, the study hopes to offer better treatment options that might reduce pain and improve the function of the elbow and shoulder in affected individuals. Participants in the study will undergo a specified treatment involving physical therapy techniques targeting the neck and upper back regions. The researchers will measure how this treatment affects the structure of the tendons and blood flow in the affected area by using ultrasound technology. They will also assess changes in pain levels and the ability to perform tasks using the shoulder and elbow. Before and after participating in the study, the strength of the hand muscles and pain levels will be evaluated to determine the effectiveness of the treatment. This comprehensive approach aims to provide a clearer understanding of how these interventions might help alleviate symptoms and improve daily functioning for those with medial epicondylitis.

Official TitleUltrasonographic Response to Cervical and Upper Thoracic SNAG in Treatment of Chronic Medial Epicondylitis, Randomized Clinical Trial
NCT07187102
Principal SponsorBeni-Suef University
Study ContactSahar M Abdelmutilibe, PHD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

60 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 35 to 50 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Elbow TendinopathyElbow InjuriesArm InjuriesMuscular DiseasesMusculoskeletal DiseasesTendon InjuriesWounds and InjuriesTendinopathy

Criteria

Inclusion Criteria: * Age ranges from 35 to 50 years old in both sexes. * Patients with LE that diagnosed by orthopedist. * Pain onset is more than 3 months appear primarily with use or rest or in both, also , it appear with deep palpation of the medial epicondyle . Exclusion Criteria: * • Rheumatoid Arthritis . * Skin infection. * History of previous elbow surgery. * Any pathology in the shoulder joint. * Neurologic deficit in upper extremity. * Cervical disc prolapse and radiculopathy C5,6. * Dislocation of elbow joint. * Recent fractures of upper extremity. * Arthrosis of the radiohumeral joint. * Osteochondritis dissecans. * Osteonecrosis. * Plica synovialis. * Participants receiving other treatment, in the form of physical therapy or medication, for the duration of the study that may interfere with the results of this study.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Participants will receive the physiotherapy traditional treatment program (4weeks, supervised sessions 3 times per week )

Group II

Experimental
Participants will receive the physiotherapy SNAG plus traditional treatment program (4weeks, supervised sessions 3 times per week )

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Faculty of Physical Therapy, Beni-Suef University

Banī Suwayf, EgyptOpen Faculty of Physical Therapy, Beni-Suef University in Google Maps
Recruiting
One Study Center