About this trial
The purpose of this feasibility study is to determine if a new emerging technology called photoacoustic tomography (PAT) can be adapted for use in humans for the detection of chronic rheumatoid arthritis.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Men and women 18 years of age or older can participate in this study.
Patients can participate in this study if they have had rheumatoid arthritis for more than 2 years and their rheumatologist has referred them to this study.
Patients can participate as a healthy volunteer with a known history of rheumatoid arthritis.
Disqualifiers
Patients, who have electrically, magnetically or mechanically activated implants such as heart pacemaker, magnetic surgical clips, prostheses or implanted neurological stimulator.
Pregnant patients.
Patients who is claustrophobic.
Patients with impaired renal function cannot participate in this study such as elevate creatinine clearance, patients on kidney dialysis etc.
Trial population
Subjects are 1) people who are either healthy volunteers or have patients who have rheumatoid arthritis for more than 2 years and who have a rheumatologist who referred them to this study.
Trial design
Cohort
Prospective
Treatments tested in this trial
Laser Based Photoacoustic Tomography, MRI, Ultrasound
Procedure/SurgeryHealthy subjects will have scans on finger joints with any of the scanning methods described above.
laser based photoacoustic tomography, MRI, ultrasound
Procedure/SurgerySubjects with arthritis will have scans on finger joints with any of the scanning methods described above.
Treatment groups
Trial outcomes
Primary outcomes
Photoacoustic Imaging
To determine if photoacoustic imaging (PAT) can accurately assist in the diagnosis of chronic rheumatoid arthritis, with data collected every 2 weeks for a maximum of 10 weeks.
Sponsors and contacts
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University of Michigan
Lead sponsor
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Collaborator