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NCT03616340 Clinical Trial

Efficacy of Intra-articular NSAID Versus Corticosteroid in the Treatment of Shoulder and Knee Conditions: A Randomized, Double-Blind, Prospective Study

Rotator Cuff Tear Clinical Trial

Official title:
Efficacy of Intra-articular NSAID Versus Corticosteroid in the Treatment of Shoulder and Knee Conditions: A Randomized, Double-Blind, Prospective Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03616340
Other study ID # 1209087-1
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date August 2018
Est. completion date August 2020

Study information
Verified date July 2018
Source OSF Healthcare System
Contact Miguel ramirez, MD
Phone 17857661273
Email maramirez09@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The proposed study will compare the efficacy of Triamcinolone versus Ketorolac for intra-articular injection of the knee and shoulder

Description:

This study will be a randomized prospective study comparing Triamcinolone to Ketorolac for injections in the knee and shoulder for a variety of orthopedic conditions. The investigators will monitor pain relief, length of pain relief, cost, and patient satisfaction after the injections

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date August 2020
Est. primary completion date August 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- knee and shoulder arthritis

- shoulder impingement

- rotator cuff tear

Exclusion Criteria:

- chronic pain management

- allergy to NSAIDs or steroids

- prior surgery

- kidney disease that would preclude NSAID administration

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Shoulder injection
intra articular or subacromial shoulder injection
• knee injection
intra-articular knee injection

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
OSF Healthcare System

Outcome
Type Measure Description Time frame Safety issue
Primary Pain level: VAS score VAS score 0-6 months
Primary length pain relief length of time patient reports pain relief 0-6 months
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