PET MRI for Evaluation of Knee Osteoarthritis in Patients With Bilateral Knee OA
NCT ID: NCT03174080
Last Updated: 2017-06-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
150 participants
OBSERVATIONAL
2017-07-16
2018-07-31
Brief Summary
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In this study, patients who suffer from two knees or unilateral pain, will take part. Participants will undergo a clinical examination, including evaluation of symptoms by an orthopedist and an X-ray imaging, which are part of the currently accepted medical diagnosis.
Patients will perform PET-MRI test in order to assess whether PET MRI is a more efficient tool for active knee osteoarthritis diagnosis.
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Detailed Description
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The purpose of this study is to examine the value of PET MRI as a tool for accurate diagnosis of active knee osteoarthritis.
The hypothesis is that using PET MRI of both knees may correlate better than radio graphs or MRI by themselves to patient symptoms .
The study will consist of 150 patients with bilateral or unilateral knee pain with one of the knees having more symptoms than the other. The study physicians who perform the PET MRI will be blinded to the patient symptoms and will record their findings and which knee is more symptomatic and along which pattern
Enrollment:
* All patients that are sent for knee MRI
* Patients over the age of 50 years old
* All patients will sign an informed consent for the study prior to the PET MRI
* Unilateral or Bilateral knee pain
* All patients were ambulatory preoperative, using no more then a single cane
* All patients had prior Weight Bearing AP x-rays and Lateral radiography The patients will be fill in SF-36 and WOMAC and VAS scores along prior to their examination.
All patients will have an orthopedic assessment of their symptoms prior to their PET MRI.
Participants will carry out a PET-MR imaging. PET involves injecting FDG (glucose labeled isotope of fluorine) intravenously at a dose of 2.5 mci . After a wait of about 40 minutes will be performed PET MR lasting up to 40 minutes.
All findings will be evaluated.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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FDG (glucose labeled isotope of fluorine)
Patients will receive an intravenous injection of 2-5mCi of 18F-FDG prior to PET MRI
Eligibility Criteria
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Inclusion Criteria
* Patients over the age of 50 years old
* All patients will sign an informed consent for the study prior to the PET MRI
* Unilateral or Bilateral knee pain
* All patients were ambulatory pre-operatively, using no more then a single cane
* All patients had prior Weight Bearing AP x-rays and Lateral Radiogrphs
Exclusion Criteria
2. History of knee arthroscopy or other surgery 1 year before the MRI
3. Bone scan performed in the past 3 months prior to the PET MRI
4. Clastrophobia
50 Years
85 Years
ALL
No
Sponsors
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Assuta Medical Center
OTHER
Responsible Party
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david groshar
Pro. David Groshar
Other Identifiers
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Assuta MC
Identifier Type: -
Identifier Source: org_study_id
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