NCT07657637

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.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress27%
Jun 2026Oct 2026

First Submitted

Initial submission to the registry

June 14, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 18, 2026

Completed
12 days until next milestone

Study Start

First participant enrolled

June 30, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2026

Last Updated

June 18, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 14, 2026

Last Update Submit

June 14, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • subacromial space

    before the first session and after the last session ( four weeks)

  • shoulder pain

    shoulder pain will be measured by numerical pain scale

    before the first session and after the last session ( four weeks)

Secondary Outcomes (1)

  • shoulder function

    Time Frame: before the first session and after the last session ( four weeks)

Study Arms (2)

sodium diclofenac radial shock wave Phonophoresis plus conventional physical therapy

EXPERIMENTAL

sodium diclofenac radial shock wave Phonophoresis plus conventional physical therapyc

Device: sodium diclofenac radial shock wave phonophoresis plus conventional physical therapy

radial shock wave plus conventional physical therapy

ACTIVE COMPARATOR

radial shock wave plus conventional physical therapy

Device: radial shock wave therapy plus conventional physical therapy

Interventions

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).

sodium diclofenac radial shock wave Phonophoresis 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).

radial shock wave plus conventional physical therapy

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Modern University for Technology and Information, Cairo, , Egypt

Cairo, Egypt

Location

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Central Study Contacts

radwa fayek lecturer, Phd

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of basic science department faculty of physical therapy

Study Record Dates

First Submitted

June 14, 2026

First Posted

June 18, 2026

Study Start

June 30, 2026

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 30, 2026

Last Updated

June 18, 2026

Record last verified: 2026-06

Locations