The effect of local injection of ozone, corticosteroid and prothorectropy under ultrasound guidance in the treatment of inflammation of shoulder tendons

Phase 3

Recruiting

• Conditions: Inflammation of the shoulder tendons.; Mononeuropathy in diseases classified elsewhere

• Registration Number: IRCT20151017024572N17
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

The presence of tandinopathy in patients as a positive one in a special shoulder test, including: Neer test, Hawkins test
Visual Analog Scale (VAS) above 4
Patient's desire to attend research project

Exclusion Criteria

Existence of a history and examination of rotator cuff tears, diabetes, coagulation disorders, fractures, rheumatologic diseases, tumors and infection
Receiving injection in the shoulder joint in the last 3 months
Frozen Shoulder
Presence of c6-c5 synchronous radiculopathy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score based on Visual Analogue Scale. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: Visual Analog Scale (VAS).;Shoulder pain and disability. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: Shoulder pain and disability index (SPADI).

Secondary Outcome Measures

Name	Time	Method
Clinical Global Impression. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: Clinical Global Impression Questionnaire.;Patient Global Impression of Improvement. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: Patient Global Impression of Improvement Questionnaire.;Shoulder rang of motiom. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: goniometer.;Synovial thickness. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: sonography.;Partial tearing. Timepoint: Before injection, 1 weeks and 8 weeks after injection. Method of measurement: sonography.;Liquid Thickness. Timepoint: Before injection, 2 weeks and 8 weeks after injection. Method of measurement: sonography.