- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01654198
PET/CT in Psoriatic Arthritis
December 7, 2020 updated by: University of Pennsylvania
FDG-PET/CT in the Diagnosis and Monitoring of Psoriatic Arthritis
When patients with psoriasis develop joint pain, it is often hard to decide whether or not the pain is due to psoriatic arthritis (PsA).
At this time, doctors use information from the history and physical exam to determine the diagnosis.
X-rays, magnetic resonance imaging (MRI) and ultrasound have been used to help with the diagnosis but all three have limitations.
A newer imaging technique, whole body Positron Emission Tomography/Computed Tomography (PET/CT) uses the idea that inflammatory cells take up sugar to locate inflammation in the body.
Because patients with PsA have inflammatory cells in their joints and tendons, this type of scan allows the physician to take a picture of the whole body and locate inflammation.
The investigators have found that some patients with psoriasis (but without arthritis) have inflammation in joints and tendons even before the patient has symptoms.
In this study, the investigators will explore how well PET/CT works for assessing inflammation in patients with PsA.
This would be a very exciting tool that could be used to find and treat inflammation before it causes damage or pain.
Study Overview
Study Type
Observational
Enrollment (Actual)
12
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania Division of Rheumatology
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with psoriatic arthritis defined by CASPAR criteria and active joint disease.
Description
Inclusion Criteria:
- Age 18-80,
- active psoriatic arthritis (joint or enthesis inflammation)
Exclusion Criteria:
- Diabetes,
- pregnant,
- no active PsA
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Psoriatic arthritis
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FDG-PET/CT is a type of imaging used currently to look for cancer.
We are using it to look at inflammation within the joints.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Primary outcome is inflammation as measured by SUVmax and metabolic volumetric product in the joints and entheses.
Time Frame: At the discretion of the PI
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At the discretion of the PI
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Correlation of local inflammation in joints and enthesis with systemic inflammatory markers including IL6 and high sensitivity CRP.
Time Frame: At the discretion of the PI
|
At the discretion of the PI
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Alexis R Ogdie, MD, MSCE, University of Pennsylvania
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2012
Primary Completion (Actual)
October 2, 2018
Study Completion (Actual)
October 2, 2018
Study Registration Dates
First Submitted
July 27, 2012
First Submitted That Met QC Criteria
July 30, 2012
First Posted (Estimate)
July 31, 2012
Study Record Updates
Last Update Posted (Actual)
December 8, 2020
Last Update Submitted That Met QC Criteria
December 7, 2020
Last Verified
December 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 815253
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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