Recruiting PHASE1 Rheumatoid Arthritis

New treatment option for Rheumatoid Arthritis

Official title Imaging of Lymphatic Vessels in People With Rheumatoid Arthritis (RA)

ClinicalTrials.gov ID: NCT05197530

What this study is testing

What is Indocyanine green?

Indocyanine green is an investigational medicine, being studied as a potential treatment for rheumatoid arthritis.

Also referred to as ICG, IC-Green.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
Lymphatic transport was previously examined by these investigators using Near InfraRed Indocyanine Green fluorescence imaging (NIR-ICG) of the upper extremities. They established reliable and reproducible methodologies in RA patients.
  • Phase 1: an early, usually small safety study

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Early RA
  • Ability to provide written informed consent
  • people must be 18 years old or older
  • RA people must fulfill 2010 American College of Rheumatology (ACR) criteria with a DAS28-C-Reactive Protein (CRP) \>3.5
  • Must have 1 year or less of disease

You likely can't join if

  • All PATIENTS
  • Active systemic disorders or inflammatory conditions other than RA, (i.e., chronic infections with hepatitis B, hepatitis C or HIV) that would...
  • Known sensitivity to iodine because of residual iodide in Indocyanine Green
  • Pregnant women should not participate; pregnancy tests will not be performed
  • Inability to donate blood due to poor venous access
See the full eligibility criteria
Who can join
  • Early RA
  • Ability to provide written informed consent
  • people must be 18 years old or older
  • RA people must fulfill 2010 American College of Rheumatology (ACR) criteria with a DAS28-C-Reactive Protein (CRP) \>3.5
  • Must have 1 year or less of disease
  • Must be MTX inadequate responder (DAS28-CRP \>2.6 at 4 months of therapy) OR experience a flare on MTX (self-reported and score of \>25 on the Outcome Measures in Rheumatology (OMERACT) Flare questionnaire AND are...
  • Must have active synovitis in one or both hands confirmed by ultrasound Established RA
  • Ability to provide written informed consent
  • people must be 18 years of age or older
  • RA people must fulfill 2010 ACR criteria with a DAS-CRP \>3.5
  • Must have at least 10 years of disease
  • Must have active synovitis in one or both hands confirmed by ultrasound
  • Must be on a stable dose of DMARD (MTX, leflunomide, azulfidine, hydroxychloroquine), Janus Kinase (JAK) inhibitor or biologic agent for 8 weeks
What rules you out
  • All PATIENTS
  • Active systemic disorders or inflammatory conditions other than RA, (i.e., chronic infections with hepatitis B, hepatitis C or HIV) that would confound the study results.
  • Known sensitivity to iodine because of residual iodide in Indocyanine Green
  • Pregnant women should not participate; pregnancy tests will not be performed
  • Inability to donate blood due to poor venous access

The study team makes the final eligibility decision.

Where it's taking place

  • Rochester, New York, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Rochester, New York, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.