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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06386926
Other study ID # P.T.REC/012/005075
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2024
Est. completion date September 2024

Study information

Verified date April 2024
Source Cairo University
Contact Shady Alkadry
Phone +201128398533
Email shad.bahaa@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparative study to compare the effect of radial shockwave versus ultrasound phonophoresis in management of chronic supraspinatus tendinitis consists of 3 groups exp1(shockwave treatment + conventional physical therapy) , exp2( ultrasound phonophoresis+ conventional physical therapy) and control group ( conventional physical therapy)


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 69
Est. completion date September 2024
Est. primary completion date July 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:- BMI 18.5-24.9 - 18 years to 60 - with Unilateral Chronic Supraspinatus Tendinitis. - Tenderness is found over the supraspinatus as it passes sub-acrominal and anterolateral. - The patient reported with positive Jobe's test (empty can test) - The patient reported pain with active shoulder elevation in the scapular plane (eg: welders, plate workers, slaughterhouse workers and overhead playing athletes). - The patient reported pain with resisted isometric abduction Exclusion Criteria: - Case reports, treatments after surgery, did not meet our specified outcome parameters, traumatic incidents, - Partial tears at surgery - Massive retracted tears at surgery - Frozen shoulder. - Rotator cuff tear. - Glenohumeral or acromioclavicular arthritis

Study Design


Intervention

Other:
Electro Therapy
radial shockwave 3 sessions one session per week for four consecutive weeks ,receive Ultrasound phonophoresis using diclofenac Na+ 12 session, 3 sessions per week and conventional physical therapy modalities in the form of 3 sessions every week for 8 weeks

Locations

Country Name City State
Egypt Cairo university Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in the thickness of supraspinatus tendon Ultrasonography before start of treatment and 4 weeks following end of treatment
Primary change in pain intesity VAS ( visual analog scale score) before start of treatment and 4 weeks following end of treatment , score from 0-10 ,0=no pain , 10= unbearable pain
Primary Change in shoulder range of motion electro goniometer before start of treatment and 4 weeks following end of treatment
Secondary Function of the Upper Limb Quick DASH Questionnaire score before start of treatment and 4 weeks following end of treatment, it measure the disability/symptom section (11 items, scored 1-5)
Secondary measure weight in kg and height in cm Weight and height scale for determining BMI before starting the assessment
See also
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Completed NCT03184181 - Application of Percutaneous Electrolysis, Percutaneous Neuromodulation and Eccentric Exercise N/A
Withdrawn NCT05184985 - TrueRelief Efficacy for Supraspinatus Tendonitis N/A
Completed NCT05241977 - MINIMUM EFFECTIVE VOLUME OF BUPIVACAİNE FOR ANTERIOR SUPRASCAPULAR NERVE BLOCK
Completed NCT05793918 - Percutaneous Electrolysis, Ultrasound-guided Percutaneous Neuromodulation Therapy and Eccentric Exercise in Supraspinatus Tendinopathy. N/A
Not yet recruiting NCT05192746 - Radial Extracorporeal Shock Wave Therapy Versus High Power Pain Threshold Ultrasound Therapy in Supraspinatus Tendinitis N/A
Completed NCT04851951 - Platelet Rich Plasma (PRP) One-Shot Injection For Supraspinatus Tendinosis
Completed NCT03744195 - Effect of Kinesotaping on Management of Supraspinatus Tendinitis N/A