Clinical Trials Directory

Trials / Unknown

UnknownNCT05818111

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
86 (estimated)
Sponsor
Taipei Veterans General Hospital, Taiwan · Other Government
Sex
All
Age
35 Years – 65 Years
Healthy volunteers
Not accepted

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

Detailed 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

Conditions

Interventions

TypeNameDescription
DRUGsteroidtriamcinolone 40mg 4cc
DRUGXylocaine 2 % Injectable Solutionxylocaine 2% 4cc
DRUGNormal saline 2ccnormal saline 2cc
DRUGnormal saline 12ccnormal saline 12cc

Timeline

Start date
2023-01-31
Primary completion
2024-01-31
Completion
2024-02-01
First posted
2023-04-18
Last updated
2023-04-18

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT05818111. Inclusion in this directory is not an endorsement.