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Clinical Trials/NCT01495455
NCT01495455
Completed
Not Applicable

Nottingham Osteoarthritis Biomarker Study 2011

University of Nottingham1 site in 1 country140 target enrollmentFebruary 2012
ConditionsOsteoarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis
Sponsor
University of Nottingham
Enrollment
140
Locations
1
Primary Endpoint
Difference in the levels of pro-inflammatory and anti-inflammatory lipids mediators between individuals with knee osteoarthritis and those with normal knees.
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Osteoarthritis is by far the most common joint condition and the single largest cause of disability in the older population. The investigators still have a poor understanding of the nature of osteoarthritis and factors that influence its development and progression. Identification of biochemical markers that relate to cartilage loss, bony overgrowth and other features that occur with osteoarthritis will advance our understanding. Over the last 5 years analytical methods have developed to measure a range of different biomarkers. This pilot study will use these analytical methods to measure biomarker levels in joint fluid, urine and blood of 50 participants with Osteoarthritis (OA) and 50 healthy volunteers.

This study will provide novel pilot data on the changes in the composition of the synovial fluid, urine and blood in patients with OA. Apart from being a key target site for OA, the knee is a suitable joint for study because of its accessibility to clinical assessment, joint aspiration and imaging.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
January 2013
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All participants:
  • Be able to provide written informed consent
  • Aged 30 and over
  • Knee OA patients:
  • Radiographic signs of OA - that is definite joint space narrowing plus osteophyte in at least one compartment of the knee
  • Normal controls:
  • No knee pain
  • No clinical or radiographic changes of knee OA

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Difference in the levels of pro-inflammatory and anti-inflammatory lipids mediators between individuals with knee osteoarthritis and those with normal knees.

Time Frame: within 6 months of recruitment of last participant

Study Sites (1)

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