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
| Type | Name | Description |
|---|---|---|
| DRUG | steroid | triamcinolone 40mg 4cc |
| DRUG | Xylocaine 2 % Injectable Solution | xylocaine 2% 4cc |
| DRUG | Normal saline 2cc | normal saline 2cc |
| DRUG | normal saline 12cc | normal 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.