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Laser-based Photoacoustic Tomography of Human Inflammatory Arthritis

Laser-based Photoacoustic Tomography of Human Inflammatory Arthritis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00748254
Enrollment
113
Registered
2008-09-08
Start date
2011-12-01
Completion date
2027-01-01
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Rheumatoid

Keywords

Rheumatoid arthritis

Brief summary

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.

Detailed description

The objective of this proposal is to adapt photoacoustic tomography (PAT), a novel, nonionizing, noninvasive, laser-based technology, for structural and functional imaging of human peripheral joints affected by inflammatory arthritis. Combining the advantages of both light and ultrasound scanning, PAT holds promise to present objective optical information in subsurface joint tissues with high sensitivity and high spatial resolution. This could be of considerable help in the early detection of inflammatory joint diseases. PAT may also prove useful in further understanding the pathophysiology of these disorders and assisting with therapeutic decisions, including assessment of new pharmacological therapies. In January 2026, the decision was made to reopen recruitment for this study to collect additional data to support future clinical trial work and funding.

Interventions

PROCEDURELaser Based Photoacoustic Tomography, MRI, Ultrasound

Healthy subjects will have scans on finger joints with any of the scanning methods described above.

PROCEDURElaser based photoacoustic tomography, MRI, ultrasound

Subjects with arthritis will have scans on finger joints with any of the scanning methods described above.

Sponsors

University of Michigan
Lead SponsorOTHER
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* 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. * Patients with shock hypotension or unstable low blood pressure. * Patients with Rhabdomyolysis. * Patients who have had a contrast enhanced (with gadolinium) MRA (magnetic resonance angiography)/ or MRI within the last 3 months. (Contrast is a medication injected into a vein during a imaging examination that helps produce clearer images/pictures).

Design outcomes

Primary

MeasureTime frameDescription
Photoacoustic Imaging10 weeksTo 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.

Countries

United States

Contacts

CONTACTSafa Mohamed
safam@med.umich.edu734 615-1646
PRINCIPAL_INVESTIGATORXueding Wang, Ph.D

University of Michigan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026