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Effect of Extracorporeal Radial Shock Wave Phonophoresis on Subacromial Space in Patients With Impingement Syndrome.

Effect of Extracorporeal Radial Shock Wave Phonophoresis on Subacromial Space in Patients With Impingement Syndrome: Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07510399
Enrollment
70
Registered
2026-04-03
Start date
2026-03-10
Completion date
2026-05-30
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impingement Syndrome, Rehabilitation, Shock Wave

Keywords

shock wave

Brief summary

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

patients will receive radial shock wave Phonophoresis by ibuprofen in the form of 2000 shocks, 2 bars, 8 MHz frequency plus (strengthening and stretching exercises for subraspinatus muscle).

DEVICEradial shock wave therapy plus conventional physical therapy.

patients will receive radial shock wave therapy ( 2000 shocks, 2 bars, 8 MHz), plus conventional physical therapy (strengthening and stretching exercises for subraspinatus muscle).

Sponsors

MTI University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
subacromial spacebefore the first session and after the last session ( four weeks)subacromial space will be measured by X ray

Secondary

MeasureTime frameDescription
shoulder painbefore the first session and after the last session ( four weeks)shoulder pain will be measured by numerical pain scale
shoulder functionbefore the first session and after the last session ( four weeks)function will be measured by shoulder pain and disability index

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026