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RecruitingNCT00748254Updated Jan 23, 2026

Laser-based Photoacoustic Tomography of Human Inflammatory Arthritis

An observational study in Arthritis, Rheumatoid, sponsored by University of Michigan. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-23.

Sponsored by University of Michigan · Observational

From the registry’s dates

  • Started Dec 2011; still recruiting 14 years 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
113
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Arthritis, Rheumatoid

Keywords

  • Rheumatoid arthritis
03

In context

Arthritis, Rheumatoid

2,888 studies on the registry are indexed under Arthritis, Rheumatoid; 390 are open to participants now.

This study's planned enrollment of 113 is below the median of 176 across 824 observational studies indexed under Arthritis, Rheumatoid.

Browse Arthritis, Rheumatoid studies →

Lead sponsor

University of Michigan is the lead sponsor of 1,475 studies on the registry; 196 are open to participants now.

Of its 162 completed or terminated interventional studies of FDA-regulated products, 128 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study 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.

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

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).
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
113 participants (estimated)
Patient registry
No

Groups and cohorts

  • Rheumatoid Arthritis

    Patients who have active disease affecting the joints in the hand will have Laser Based Photoacoustic Tomography (PAT), MRI, Ultrasound

    Procedure: Laser Based Photoacoustic Tomography, MRI, Ultrasound

  • Normal controls

    Healthy volunteers who do not have arthritis will also have Laser Based Photoacoustic Tomography (PAT), MRI, Ultrasound on the joints of their hand

    Procedure: laser based photoacoustic tomography, MRI, ultrasound

Interventions

  • ProcedureLaser Based Photoacoustic Tomography, MRI, Ultrasound

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

    Also known as: MRI,magnetic resonance imaging, US, ultrasound, PAT, laser based photoacoustic tomography

  • Procedurelaser based photoacoustic tomography, MRI, ultrasound

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

    Also known as: laser based photoacoustic tomography, MRI, Ultrasound

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 10 weeks

07

Study locations

1 of 1 sites recruiting
  • Universtity of Michigan Health System
    Ann Arbor, Michigan 48109, United States
    • Xueding Wang, PHD · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00748254
Lead sponsor
University of Michigan
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Responsible party
Xueding Wang (Principal Investigator, University of Michigan) — Principal investigator
First posted
Sep 8, 2008
Start date
Dec 1, 2011
Primary completion
Jan 2027 (estimated)
Completion
Jan 2027 (estimated)
Last update
Jan 23, 2026

Study contacts

Safa Mohamed
Contact
safam@med.umich.edu
734 615-1646
Xueding Wang, Ph.D
principal investigator · University of Michigan

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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