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Clinical Trials/NCT02829463
NCT02829463
Completed
Not Applicable

Magnetic Resonance Imaging of Infrapatellar Fat Pad in Osteoarthritis and Controls

The Third Xiangya Hospital of Central South University1 site in 1 country121 target enrollmentOctober 2015
ConditionsOsteoarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis
Sponsor
The Third Xiangya Hospital of Central South University
Enrollment
121
Locations
1
Primary Endpoint
Infrapatellar Fat Pad Volume in MRI
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

In this study, the investigators use the clinical documentation and imaging data of MRI to do research. Clinical subjects were divided into two groups: osteoarthritis patients and healthy controls without osteoarthritis. Differences of MRI data were studied between two groups.

Detailed Description

In this study, the investigators applied high precision MRI technique (with as less as a slice thickness of 0.35 mm and without inter-slice gap), and calculated not only the IPFP maximal sagittal area and IPFP volume, but also the quantitated signal, and compared the differences between healthy controls and osteoarthritis patients. This is an observational cross-sectional study without specific interventions to the subjects. MRI is a regular examination in our hospital. And all subjects are included for the reasons of osteoarthritis (need MRI) and healthy controls (pain but not osteoarthritis, also need MRI). The investigator does not assign specific interventions to the subjects of the study.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
July 2016
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients with clinical knee osteoarthritis;
  • The healthy controls who require MRI test.

Exclusion Criteria

  • Contraindications to magnetic resonance imaging;
  • Rheumatoid arthritis patients;
  • Hemophilic arthritis;
  • Subjects who take non-steroidal anti-inflammatory drugs (NSAIDs);
  • Subjects who take lipid-lowering agents;
  • Subjects who have the history of knee trauma;
  • Subjects who have the history of knee operation;
  • Subjects who have the disease of musculoskeletal tumor near knee;
  • Subjects who have joint loose bodies.

Outcomes

Primary Outcomes

Infrapatellar Fat Pad Volume in MRI

Time Frame: collect the data within 24 hours after the subjects did the MRI

Study Sites (1)

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