Efficacy of Diclofenac Sodium Shock Wave Phonophoresis on Patients With Subacromial Impingement Syndrome
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: sodium diclofenac radial shock wave phonophoresis plus conventional physical therapy, radial shock wave therapy plus conventional physical therapy.
- Who it may be relevant to
- Registry conditions: Shock Wave, Subacromial Impingement Syndrome. Basic parameters: 25 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Efficacy of Diclofenac Sodium Shock Wave Phonophoresis on Patients With Subacromial Impingement Syndrome: A Randomized Controlled Trial
Overview
The goal of the study is to determine the effect of radial shock wave Phonophoresis on patients with impingement syndromes. to answer the following questions: does shock wave Phonophoresis have and effect on pain? does shock wave Phonophoresis have and effect on shoulder function? does shock wave Phonophoresis have and effect on subacromial space? patients will be randomized to two groups: Group (A): patients will receive shock wave Phonophoresis plus conventional physical therapy. Group (B): Patients will receive shock wave plus conventional Physical therapy.
Interventions
- Device sodium diclofenac radial shock wave phonophoresis plus conventional physical therapy
patients will receive radial shock wave Phonophoresis by ibuprofen in the form of 2000 shocks, 2.4 bars, 10 MHz frequency plus (strengthening and stretching exercises for subraspinatus muscle). - Device radial shock wave therapy plus conventional physical therapy
patients will receive radial shock wave therapy ( 2000 shocks, 2.4 bars, 10 MHz), plus conventional physical therapy (strengthening and stretching exercises for subraspinatus muscle).
Primary outcome measures
- subacromial space [Time frame: before the first session and after the last session ( four weeks)]
- shoulder pain [Time frame: before the first session and after the last session ( four weeks)]
Secondary outcome measures (1)
- shoulder function [Time frame: Time Frame: before the first session and after the last session ( four weeks)]
Eligibility criteria
Inclusion criteria
- Patients age range between 25-40 years ago.
- Shoulder pain between 60- 120° with shoulder elevation (positive painful arch test).
- Grade 2 impingement syndrome according to neer classification.
Exclusion criteria
- Shoulder affected bilaterally
- Receiving anesthetic or corticosteroid injections within 4 weeks of study enrollment
- Surgery or previous fractures of the ipsilateral humeral head of the affected shoulder
- Osteoarthritis in the acromioclavicular or glenohumeral joints
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Modern University for Technology and Information, Cairo, , Egypt — Cairo
Identifiers
NCT: NCT07657637 · Pending