Ultrasonographic Response to Cervical and Upper Thoracic SNAG in Medial Epicondylitis, Randomized Clinical Trial

NCT ID: NCT07187102

Last Updated: 2025-09-22

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-08
• Study Completion Date: 2025-11-01

Brief Summary

Aim of the work :

1. To detect if there is any change would occur in the neovascularity and echogenicity after using cervical and upper thoracic SNAG or not in ME patients.

2. To find the effect of cervical and upper thoracic SNAG on pain, function of upper extremities, grip strength in ME comparing with traditional treatment alone

Detailed Description

medial epicondylitis(ME) of the elbow is a condition characterized by aggravation of pain in the outer part of the elbow during active wrist flexion , and presentation of pain on direct palpation of the medial epicondyle, or proximal muscle belly . Biomechanical and sensorimotor deficits can occur and adversely impact upper extremity function .These functional deficits may interfere with occupational tasks and activities of daily living The study's results: Measuring the changes that will be produced by using therapeutic growth of the cervical and thoracic vertebrae on the pathological changes that persist in the tendons of the tens of the tibialis cruciate ligaments in detecting excess weight resulting from the disease of the middle epicondyle, such as increased blood vessels in the tendon and decreased echogenicity of the tendon, in addition to measuring the changes that occurred in the extent of pain sensation and the extent of functional performance of the shoulder and elbow joints. Patients will be directly selected jointly according to the patient's specifications for the research and written consent will be obtained from the patient after a detailed explanation of the research steps and what is required of him. The vocal function of the tendon will be evaluated, with the exception of functional pain of the successful upper extremity and the strength of the hand muscles before and after the experiment.

Conditions

Medial Epicondylitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

experimental group

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

Group Type: EXPERIMENTAL

SNAG ( sustained natural apopheseal glide )

Intervention Type: OTHER

SNAG : type of mobilization of vertebral coulmn

control group

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

Group Type: OTHER

SNAG ( sustained natural apopheseal glide )

Intervention Type: OTHER

SNAG : type of mobilization of vertebral coulmn

Interventions

SNAG ( sustained natural apopheseal glide )

SNAG : type of mobilization of vertebral coulmn

Intervention Type: OTHER

Eligibility 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.

• Minimum Eligible Age: 35 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beni-Suef University

OTHER

Sponsor Role: lead

Responsible Party

Sahar Mowad Abdelmutilibe

faculty of physical therapy , beni suef university

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Faculty of Physical Therapy, Beni-Suef University

Banī Suwayf, , Egypt

Site Status: RECRUITING

Countries

Egypt

Central Contacts

Sahar M Abdelmutilibe, PHD

Role: CONTACT

sahar.mowad@pt.bsu.edu.eg

0021027620061

Facility Contacts

Sahar M Abdelmutilibe

Role: primary

sahar.mowad@pt.bsu.edu.eg

0021027620061

Other Identifiers

FMBSUREC/07092025/Ahmed

Identifier Type: -

Identifier Source: org_study_id