- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06342518
ESWT in Lateral Epicondylitis: Clinical,Ultrasonographic Evaluation
Clinical and Sonographic Evaluation of the Effectiveness of Extracorporeal Shock Wave Therapy (ESWT) in Patients With Lateral Epicondylitis
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey, 34732
- Istanbul Medeniyet University Faculty of Medicine, Physical Medicine and Rehabilitation Department
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- experiencing pain and tenderness in the lateral epicondyle while extending their wrist and fingers against resistance for at least 3 months
Exclusion Criteria:
- Patients who are pregnant or have a coagulation disorder, cervical radiculopathy, peripheral neuropathy, peripheral vasculopathy in the upper extremity, complex regional pain syndrome, local infections, systemic inflammatory disease, fibromyalgia syndrome, arthritis (including rheumatoid arthritis, spondylarthritis, and crystal-induced arthropathies), malignancy, or those who have been treated with corticosteroids, PRP, or autologous blood injection, as well as those who have received physical therapy agents, undergone upper-extremity surgical interventions, or have a history of direct trauma to the elbow or a history of fracture,
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: ESWT GROUP
The ESWT group received radial ESWT on the painful lateral epicondyle once per week for a total of 3 sessions. A wrist resting splint, wrist extensor strengthening and stretching exercises, and ice treatment were administered to both groups. |
The ESWT group received radial ESWT each session with a total of 2000 pulses at a frequency of 10 Hz.
A gel was used at the interface, and the air pressure was set at 1.8 bar per session.
Ensuring proper usage of the wrist resting splint by the patient was confirmed during follow-up visits.
The physician instructed the patients on stretching and strengthening exercises for wrist extensors, which they were asked to perform three times a day.
Application of ice for 20 minutes every 3-4 hours during painful periods was recommended.
During follow-up visits patients confirmed that they adherence to exercises and recommendations.
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Sham Comparator: Sham-ESWT group
The Sham-ESWT group received Sham radial ESWT on the painful lateral epicondyle once per week for a total of 3 sessions. A wrist resting splint, wrist extensor strengthening and stretching exercises, and ice treatment were administered to both groups. |
Ensuring proper usage of the wrist resting splint by the patient was confirmed during follow-up visits.
The physician instructed the patients on stretching and strengthening exercises for wrist extensors, which they were asked to perform three times a day.
Application of ice for 20 minutes every 3-4 hours during painful periods was recommended.
During follow-up visits patients confirmed that they adherence to exercises and recommendations.
The Sham-ESWT group received Sham radial ESWT each session, but without actual contact of the applicator.
To enhance the illusion of treatment, gel was applied, and the device emitted sound at every shock
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hand Grip Strength
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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measured using the Jamar hand dynamometer
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Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Pain severity
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Visual Analog Scale (VAS) which was scored from 0 (no pain) to 10 (extremely severe).
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Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Functionality
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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the Patient-Rated Tennis Elbow Evaluation (PRTEE) The PRTEE allows patients to rate their levels of tennis elbow pain and disability from 0 to 10, and consists of 2 subscales:
Pain Score = Sum of the 5 pain items(out of 50) Best Score = 0, Worst Score =50 Function Score = Sum of the 10 function items, Divided by 2 (out of 50) Best Score = 0, Worst Score = 50 Computing the Total Score Total Score = Sum of pain + function scores Best Score = 0, Worst Score = 50 Best Score = 0, Worst Score = 100 |
Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Quality of life score
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Short Form-12 (SF-12), Patients are provided with the SF-12 questionnaire, which consists of 12 questions covering physical and mental health domains. The scoring yields two summary measures: the Physical Component Summary (PCS) and the Mental Component Summary (MCS). PCS mean score: 56,5 MSC mean score: 60.7 Scores above mean indicate a better-than-average health-related quality of life, while scores below mean suggest below-average health. |
Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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deep muscular tissue sensitivity
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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pain pressure threshold (PPT) Pain pressure threshold (PPT) is used to measure deep muscular tissue sensitivity.
The test determines the amount of pressure over a given area in which a steadily increasing nonpainful pressure stimulus turns into a painful pressure sensation.
A varying pressure is applied from 0.5 to 1 kg/sec in a perpendicular direction relative to the muscle.
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Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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thickness of the common extensor tendon (CET)
Time Frame: Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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During ultrasonography for LE, the elbow is positioned in 90 degrees of flexion and the wrist in pronation.
The ultrasound probe is placed longitudinally on the radial surface of the elbow.
And common extensor tendon thickness was measured sonographically.
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Baseline, post-treatment(4th week), and one-month post-treatment (8th week)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MU ESWT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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