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Effect of Periarticular Prolotherapy with Dextrose in Patients with Rotator Cuff Tendonitis

Phase 3
Conditions
Rotator Cuff Tendonitis.
Incomplete rotator cuff tear or rupture not specified as traumatic
M75.11
Registration Number
IRCT20181217042028N1
Lead Sponsor
Artesh University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients with Rotator Cuff Tendonitis

Exclusion Criteria

History of Diabetes Mellitus
History of Malignancy
Complete rotator cuff tear

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain and disability severity based on Shoulder Pain and Disability Index questionnaire. Timepoint: Before the intervention, one week and a month later. Method of measurement: Shoulder Pain and Disability Index questionnaire.;Pain severity based on Visual Analogue Scale. Timepoint: Before the intervention, one week and a month later. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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