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NCT01359553 Clinical Trial

Clinical Study of Novel Diagnostic Techniques for Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

Official title:
Comparison Between Intra-articular Ultrasound Imaging, Non-invasive Ultrasound Imaging, Quantitative MRI Imaging, Contrast-enhanced CT Imaging and Arthroscopy for Diagnostics of Knee Osteoarthritis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01359553
Other study ID # UltraRusto
Secondary ID
Status Completed
Phase N/A
First received May 22, 2011
Last updated October 24, 2016
Start date May 2011
Est. completion date May 2014

Study information
Verified date October 2016
Source University of Oulu
Contact n/a
Is FDA regulated No
Health authority Finland: Ministry of Social Affairs and Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to clarify the potential of intra-articular ultrasound imaging, non-invasive ultrasound imaging, quantitative MRI imaging, contrast-enhanced CT imaging and arthroscopy for diagnostics of knee osteoarthritis. All methods will be cross-correlated and compared with the arthroscopic findings.

Recruitment information / eligibility
Status Completed
Enrollment 12
Est. completion date May 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Kellgren-Lawrence grade = 1-3 or cartilage defect detected in MRI

- Age >= 20 years

Exclusion Criteria:

- Tumor or inflammation in the knee

- Severe general diseases

- Diabetes

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• Intra-articular ultrasound imaging of knee joint during arthroscopy

• Non-invasive ultrasound imaging of knee

• Quantitative MRI imaging of knee

• Contrast-enhanced CT imaging of knee

Locations
Country Name City State
Finland Oulu University Hospital Oulu

Sponsors (4)
Lead Sponsor Collaborator
University of Oulu Kuopio University Hospital, Oulu University Hospital, University of Eastern Finland

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Arthroscopical OA grade 2014 No
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