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Comparison of Different Volume of Steroid Hydrodilatation in Treating Patients With Adhesive Capsulitis

Adhesive Capsulitis Clinical Trial

Official title:
Comparison of Different Volume of Steroid Hydrodilatation in Treating Patients With Adhesive Capsulitis

Clinical Trial Summary

This study was conducted to compare the efficacy of low volume steroid hydrodilatation with high volume steroid hydrodilatation under ultrasonographic guidance for treating adhesive capsulitis

Clinical Trial Description

adhesive capsulitis is a common cause of shoulder pain, and the efficacy of most interventions is limited. This study was conducted to compare the efficacy of low volume steroid hydrodilatation with high volume steroid hydrodilatation under ultrasonographic guidance for treating adhesive capsulitis Design: a prospective, double-blinded, randomized, clinical trial Patient and methods: Patients with adhesive capsulitis for at least 3 months were enrolled and randomly allocated into group 1 (10cc steroid hydrodilatation under ultrasonographic guidance ) and group 2 (20cc steroid hydrodilatation). The patients were evaluated before treatment and were reevaluated 0, 6, and 12 weeks after the beginning of the treatment. Outcomes measures included a pain scale (visual analog scale), range of motion, Shoulder Pain And Disability Index ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05818111
Study type Interventional
Source Taipei Veterans General Hospital, Taiwan
Contact Jia chi C Wang
Phone 0919527693
Email jcwang0726@gmail.com
Status Recruiting
Phase N/A
Start date January 31, 2023
Completion date February 1, 2024
View Details
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