Clinical Trials Directory

Trials / Completed

CompletedNCT03120923

Combined Corticosteroid With Low Volume Compared to High Volume in Impingement Syndrome

A Short Term Outcomes of Subacromial Injection of Combined Corticosteroid With Low Volume Compared to High Volume of Local Anesthetic for Rotator Cuff Impingement Syndrome: A Randomized Controlled Trials

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Ramathibodi Hospital · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

This study aims to assess and compare the effectiveness of two different volumes of local anesthetic combined with 40mg of triamcinolone for subacromial injections in treating patients with rotator cuff impingement syndrome

Detailed description

Patients with rotator cuff impingement syndrome were randomized to undergo subacromial injection with 10mL total volume of 1% lidocaine plus 40mg triamcinolone acetonide (n = 22), or a 4mL total volume of 1% lidocaine plus 40-mg triamcinolone acetonide (n = 23). Evaluations using a visual analog scale (VAS) for pain during motion, and the Western Ontario Rotator Cuff Index (WORC) were completed before treatment and 30 minutes, 2 weeks, and 8 weeks after injection.

Conditions

Interventions

TypeNameDescription
DRUGLidocaine 3 cc
DRUGLidocaine 9 cc9mL of 1% lidocaine plus 1mL of 40mg triamcinolone acetonide
DRUGTriamcinolone Acetonide

Timeline

Start date
2015-01-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2017-04-19
Last updated
2017-10-18

Source: ClinicalTrials.gov record NCT03120923. Inclusion in this directory is not an endorsement.