Investigation of three injection methods under ultrasound guidance inside the shoulder joint in patients with frozen shoulder

Not Applicable

Recruiting

• Conditions: Adhesive capsulitis of shoulder.; Adhesive capsulitis of shoulder; M75.0

• Registration Number: IRCT20230316057742N2
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 102

Inclusion Criteria

Definitive diagnosis of ice shoulder by an orthopedic doctor
Failure to respond to non-invasive treatments such as physiotherapy and drug therapy
Active and passive reduction of rom movements
Age between 18-60 years

Exclusion Criteria

known systemic diseases such as rheumatoid arthritis
History of recent trauma or surgery or known chronic disease (such as rotator cuff lesions) Pivacaine, any known systemic disease
Midclavicular joint, cervical radiculopathy
Brachial plexopathy, neoplasm
pregnancy
Addiction to opioids
diabetes
Osteoarthritis

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1) Shoulder function. Timepoint: Before the injection and during the follow-up times 2-6-12-24 weeks after the intervention. Method of measurement: 1)Checklist of movement scale (ROM) according to the study of Mardani-Kivi et al.;2)Pittsburgh Sleep Quality Index. Timepoint: Before the injection and during the follow-up times 2-6-12-24 weeks after the intervention. Method of measurement: 3)Pittsburgh Sleep Quality Index.;4) pain criterion. Timepoint: Before the injection and during the follow-up times 2-6-12-24 weeks after the intervention. Method of measurement: Visual Analog Scale.