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Rheumatoid Arthritis (RACAT-RANCT07315997

The Coronary Artery Calcium and Troponins in Rheumatoid Arthritis (CAT-RA) Study

An observational study of Rheumatoid Arthritis (RA and Atherosclerotic Cardiovascular Disease (ASCVD), run by Brigham and Women's Hospital at 3 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Individuals with rheumatoid arthritis (RA) have up to 2x the risk of having a heart attack compared to someone without RA. The goal of this study is to identify biomarkers that can help us do a better job of identifying individuals at risk before they develop symptoms of heart disease and start preventative treatment… Read more about this study

Who is it for?
Ages 35 to 79 years
What is being tested?
high sensitivity cardiac troponin
How many people
120 participants
Where
3 sitesUnited States
Study dates
4 Sep 2024to 4 Mar 2028
How long will I take part?
2 Years
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 35 to 79 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with rheumatoid arthritis, age 40- 79 years, with one cardiovascular risk factor and not on a statin or has a contraindication to statin therapy.

Who may be able to join

  • RA diagnosed by a rheumatologist
  • Age 40- 79
  • ≥1 ASCVD risk factor including prediabetes, hypertension, BMI >30, current or history of cigarette smoking

Who cannot join

  • Patients on a statin or with a contraindication to statin, on a cholesterol absorption inhibitor, or on a PCSK9 inhibitor
  • Patients with diabetes mellitus
  • Pregnancy

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

United States3 sites, 3 recruiting
  • Massachusetts General Hospital: Rheumatology

    Boston, Massachusetts, 02114

    Sheila Arvikar, MD, 6177267938, sarvikar@mgh.harvard.edu

    Abisayo Animashaun, MS, 617-732-8169, aanimashaun@mgb.org

    Recruiting
  • Brigham and Womens Hospital

    Boston, Massachusetts, 02115

    Katherine P Liao, MD, MPH, 617-525-8819, kliao@bwh.harvard.edu

    Abisayo Animashaun, MS, 617-732-8169, aanimashaun@mgb.org

    Recruiting
  • Brigham and Women's Faulkner Hospital

    Boston, Massachusetts, 02130

    Nicole Yang, MD, 6179837720, nyang2@bwh.harvard.edu

    Abisayo Animashaun, MS, 617-732-8169, aanimashaun@mgb.org

    Recruiting

Other trials in United States

About this study

Individuals with rheumatoid arthritis (RA) have up to 2x the risk of having a heart attack compared to someone without RA. The goal of this study is to identify biomarkers that can help us do a better job of identifying individuals at risk before they develop symptoms of heart disease and start preventative treatment earlier.

Read the detailed description

The objective of this study is to test the utility of high sensitivity cardiac troponin (hs-cTn) and coronary artery calcium (CAC) in risk stratifying patients with rheumatoid arthritis (RA) who may benefit from lipid lowering therapy. The population of interest are individuals who would not otherwise be recommended for therapy based on general population risk calculators for heart disease risk.

Being tested
high sensitivity cardiac troponin
Keywords
CAT-RA
Medical subject headings
Arthritis, Rheumatoid, Atherosclerosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • high sensitivity cardiac troponinDiagnostic test

    Blood measurement of high sensitivity cardiac troponin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. coronary artery calcium score

    Quantified coronary artery calcium score

    Measured: Cross-sectional, at baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jan 2026
  2. Study start4 Sep 2024
  3. Primary completion4 Mar 2028 (estimated)
  4. Study completion4 Mar 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
120 participants (estimated)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07315997
Sponsor's protocol ID
2024P001981
Acronym
CAT-RA
Status last verified
Dec 2025
First submitted
31 Dec 2025
Last updated
14 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Pending IRB approval.

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