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Effect Of Hydrocortisone Phonophoresis Versus Iontophoresis In Patients With Subacromial Impingement Syndrome

H

Horus University

Status

Enrolling

Conditions

Impingement Syndrome
Subacromial Impingement Syndrome

Treatments

Other: hydrocortisone iontophoresis
Other: Therapeutic exercise
Other: hydrocortisone phonophoresis

Study type

Interventional

Funder types

Other

Identifiers

NCT05919121
MOHSEN_IBRAHIM_phd

Details and patient eligibility

About

The purpose of this study will be to compare the efficacy of adding hydrocortisone phonophoresis or iontophoresis on pain, function, range of motion and shoulder external rotation isometric strength in patients with subacromial impingement syndrome.

Full description

Routine physiotherapy has been advocated was an effective treatment for SIS. However, there is lack of best exercise treatment and lots of studies are under consideration. According to published data focused on management of shoulder pain, it looks like that therapeutic exercise is not sufficient to treat SIS and it is compulsory to combine with other remedies to get the best results

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. All patients were diagnosed as unilateral SIS with stage II Neer classification > 3 months.
  2. Positive impingement sign (Neer's test or Hawkins-Kennedy test), / painful arc during active arm elevation, pain or weakness with resisted isometric external rotation or resisted scapular plane abduction with the humeral internal rotation (empty can test)
  3. The age of patients ranged from 18 - 60 years old.
  4. Both genders will be involved.
  5. Shoulder pain scores more than 5 on a numeric rate scale for pain of 0- 10.
  6. Failure to respond to conservative NSAID.

Exclusion criteria

  1. Frozen shoulders.
  2. Arthritis of the shoulder.
  3. Shoulder instability.
  4. Pregnant women.
  5. A pacemaker.
  6. Previous shoulder surgery.
  7. History of dislocation of the shoulder.
  8. Internal metallic fixation.
  9. Malignancy.
  10. Previous corticosteroid injection.
  11. Rheumatoid arthritis
  12. Partial or Full thickness tear of the rotator cuff.
  13. Cervical radiculopathy.
  14. Physiotherapeutic shoulder treatment within the last 3 months.
  15. The patients will randomly be assigned into 3 equal groups, 20 patients for each group.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 3 patient groups

Therapeutic exercise group
Active Comparator group
Description:
Therapeutic exercise group, group A.
Treatment:
Other: Therapeutic exercise
hydrocortisone phonophoresis group
Experimental group
Description:
This group (B) will receive the same exercise program in addition to hydrocortisone phonophoresis. Patients will receive topical medium phonophoresis of 10% hydrocortisone gel.
Treatment:
Other: hydrocortisone phonophoresis
Other: Therapeutic exercise
hydrocortisone iontophoresis group
Experimental group
Description:
This group (C) will receive the same exercise program in addition to hydrocortisone iontophoresis.
Treatment:
Other: hydrocortisone iontophoresis
Other: Therapeutic exercise

Trial contacts and locations

1

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Central trial contact

Mohsen Ibrahim

Data sourced from clinicaltrials.gov

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