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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04833738
Other study ID # Yuzuncu Yil University
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 11, 2013
Est. completion date May 28, 2014

Study information

Verified date April 2021
Source Yuzuncu Yil University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background: Electrotherapy, corticosteroid, and hyaluronic acid have been used to treat subacromial impingement syndrome. However, we need to compare treatment options to provide the optimal results. This study aims to compare the effect of hyaluronic acid, corticosteroid, and electrotherapy in subacromial impingement syndrome. Design: Ninety five patients were randomised into three equal groups according to treatment types. Hyaluronic acid (20 mg/2ml, three times one week apart) or corticosteroid (triamcinolone acetonide, 40 mg/ml, single dose) treatments were applied as subacromial injections. Electrotherapy consisted of 14 sessions TENS (20 min.), hotpack (20 min.) and ultrasound (1.5watt/cm2, 1 MHz, 6 min.). Patients were evaluated before treatment, one and four weeks post end of treatment. Visual Analogue Scale (VAS), range of motion (ROM), and Shoulder Disability Questionnaire (SDQ) were used as outcome measures.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date May 28, 2014
Est. primary completion date December 10, 2013
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - The diagnosis of subacromial impingement syndrome Exclusion Criteria: - Patients aged <20 or >50 years or who have the following medical conditions were excluded: physical therapy or injection in the past 6 months, shoulder instability, acute trauma, adhesive capsulitis, psychiatric illness, diabetes mellitus, malignancy.

Study Design


Intervention

Drug:
Hyaluronic acid

Corticosteroids Triamcinolone Acetonide
triamcinolone acetonide, 40 mg/ml, single dose
Other:
Electrotherapy
electrotherapy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Seyhmus KAPLAN

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale Higher scores represent higher level of shoulder pain. 1 min.
Primary range of motion Higher scores represent lower level of shoulder function. 5 min.
Primary Shoulder Disability Questionnaire Higher scores represent higher level of shoulder pain. 15 min
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