Cardiovascular Inflammation Reduction Trial - Inflammation Imaging Study (CIRT)
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ClinicalTrials.gov Identifier: NCT02576067 |
Recruitment Status :
Completed
First Posted : October 15, 2015
Results First Posted : April 20, 2020
Last Update Posted : April 20, 2020
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Vascular inflammation, a central feature of atherosclerosis, participates in the initiation, perpetuation and instability of plaques. Multiple clinical trials of cholesterol lowering therapy with statins have demonstrated that reductions in atherosclerotic cardiovascular disease (CVD) events are associated with reductions in both LDL cholesterol (LDL-C) and the systemic inflammatory mediator C-reactive protein (CRP). The Cardiovascular Inflammation Reduction Trial (CIRT) investigates if an anti-inflammatory agent commonly used in rheumatoid arthritis (low dose methotrexate (LDM)) can reduce CV morbidity and mortality among patients with a prior myocardial infarction or angiographically demonstrated multivessel coronary artery disease (GCO#13-1467).
In this ancillary CIRT imaging study, the investigators propose to use this well validated approach by non-invasive serial FDG-PET/CT imaging in a subset of patients enrolled in the main CIRT trial to directly visualize vascular inflammation. Once the subjects are enrolled in the main CIRT trial, baseline imaging will be done and follow up imaging will be done approximately 8 months after the baseline imaging.
18FDG-PET imaging data will be acquired, analyzed centrally and results incorporated into the main CIRT database. The investigators hypothesize that LDM treatment will result in a significant decrease in plaque inflammation as measured by 18-FDG-PET/CT after 8 months as compared to placebo.
Condition or disease | Intervention/treatment | Phase |
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Vascular Inflammation Atherosclerotic Cardiovascular Disease | Drug: Low dose methotrexate Drug: Placebo | Phase 3 |
The NHLBI funded (Ridker 5U01HL101422) Cardiovascular Inflammation Reduction Trial (CIRT) provides a unique opportunity to investigate whether a commonly used anti-inflammatory agent used in rheumatoid arthritis (low dose methotrexate (LDM)) can reduce CVD morbidity and mortality among patients with stable coronary artery disease. CIRT, is a randomized, double-blind, placebo-controlled, multi-center trial among 7,000 men and women with prior myocardial infarction or angiographically demonstrated multivessel coronary artery disease. Eligible participants will be randomly allocated over a three to four year period to usual care plus placebo or usual care plus LDM (average dose of 15-20 mg po/weekly. CIRT proposes that the reduction in CVD events with methotrexate derives from its effect on vascular inflammation, thus it is crucial to incorporate a measure of vascular inflammation imaging for confirmation of the primary mechanism of action underlying CIRT. As such, the direct evaluation of arterial inflammation would enhance the scientific value of the CIRT trial.
The inclusion of the proposed vascular inflammation imaging substudy has widespread implications that will allow this imaging modality to serve as a surrogate measure of disease, and thereby provide an opportunity for stratification in individuals at risk for CVD and evaluation of other interventions with presumed anti-inflammatory effects.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 123 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Investigator) |
Primary Purpose: | Treatment |
Official Title: | Cardiovascular Inflammation Reduction Trial (CIRT) - Inflammation Imaging Study |
Actual Study Start Date : | December 18, 2015 |
Actual Primary Completion Date : | March 29, 2019 |
Actual Study Completion Date : | March 29, 2019 |

Arm | Intervention/treatment |
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Experimental: Low dose methotrexate
average dose of 15-20 mg po/weekly
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Drug: Low dose methotrexate
Study participants will additionally receive 1 mg daily oral folate. |
Placebo Comparator: Placebo
matching placebo
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Drug: Placebo |
- Change in Arterial Inflammation [ Time Frame: baseline and 8 months ]Change in arterial inflammation - The relative change at 8 months as compared to baseline in arterial inflammation as measured by the most diseased segment (MDS) of the index vessel. The MDS is defined as the 1.5 cm segment within the carotid artery (right or left carotid) that demonstrates the highest PET/CT activity, and is calculated as a mean of maximum TBR values derived from 3 contiguous axial segments. The index vessel in turn is defined as the vessel (either aorta, right, or left carotid) with the greatest mean TBR at baseline. (MDS TBR Index Vessel)
- Change in Max Target-to-background (TBR) [ Time Frame: baseline and 8 months ]Change in max target-to-background (TBR) - The mean of max TBR within the carotid arteries as an average of the slices from the left and right carotid) at follow up imaging as compared to baseline.
- Change in Max TBR Within the Carotid Arteries [ Time Frame: baseline and 8 months ]Change in max target-to-background (TBR) - The mean of max TBR within the carotid arteries as an average of the slices from the left and right carotid)

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Age > 18 years at screening
- Documented MI in the past or past evidence of multivessel coronary artery disease by angiography must have completed any planned coronary revascularization procedures associated with the qualifying event, and must be clinically stable for at least 60 d before screening; the qualifying prior MI must be documented either by hospital records or by evidence on current electrocardiogram of Q waves in 2 contiguous leads and/or an imaging test demonstrating wall motion abnormality or scar; the qualifying documentation of multivessel coronary disease must include angiographic evidence of atherosclerosis in at least 2 major epicardial vessels defined either as the presence of a stent, a coronary bypass graft, or an angiographic lesion of 60% or greater. Left main coronary artery disease that has been revascularized with a stent or bypass graft will qualify as multivessel disease, as will the presence of a 50% or greater isolated left main stenosis.
- History of type 2 diabetes or metabolic syndrome at the time of study enrollment
- Willing to participate as evidence by signing the study informed consent
Exclusion Criteria:
- Prior history of chronic infectious disease, including tuberculosis, severe fungal disease, or known HIV positive
- Chronic hepatitis B or C infection
- Interstitial pneumonitis, bronchiectasis, or pulmonary fibrosis. Chest x-ray evidence in the past 12 months of interstitial pneumonitis, bronchiectasis, or pulmonary fibrosis.
- Prior history of non basal cell malignancy or myeloproliferative or lymphoproliferative disease within the past 5 years
- White blood cell count <3,500/mm3, hematocrit <32%, or platelet count <75000/mm3
- Liver transaminase levels (AST/ALT) greater than the upper limit of normal or albumin less than the lower limit of normal
- Creatinine clearance (CrCl) <40 mL/min as estimated by the Cockcroft-Gault equation
- History of alcohol abuse or unwillingness to limit alcohol consumption to <4 drinks per week
- Women of child bearing potential, even if currently using contraception, and women intending to breastfeed
- Men who plan to father children during the study period or who are unwilling to use contraception
- Requirement for use of drugs that alter folate metabolism (trimethoprim/sulfamethoxazoyl) or reduce tubular excretion (probenecid) or known allergies to antibiotics making avoidance of trimethoprim impossible
- Current indication for methotrexate therapy
- Chronic use of oral steroid therapy or other immunosuppressive or biologic response modifiers
- Known chronic pericardial effusion, pleural effusion, or ascites
- New York Heart Association class IV congestive heart failure
- Life expectancy of <3 years
The study population for the ancillary study will be the same as the main trial with the following additional exclusion criteria
- Subjects with a history of multiple imaging studies associated with radiation exposure
- Insulin-dependent diabetics
- If subject is Type 2 diabetic, hemoglobin A1c greater than 8% as determined by patient medical record review in the one year prior to the date of consent to this study.
- BMI greater than 37 kg/m2 or weight greater than 350 pounds

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02576067
United States, Massachusetts | |
Massachusetts General Hospital | |
Boston, Massachusetts, United States, 02199 | |
United States, New York | |
Icahn School of Medicine at Mount Sinai | |
New York, New York, United States, 10029 | |
Canada, Ontario | |
St. Michael's Hospital | |
Toronto, Ontario, Canada |
Principal Investigator: | Zahi Fayad, PhD | Icahn School of Medicine at Mount Sinai |
Documents provided by Zahi Fayad, Icahn School of Medicine at Mount Sinai:
Responsible Party: | Zahi Fayad, Director Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai |
ClinicalTrials.gov Identifier: | NCT02576067 |
Other Study ID Numbers: |
GCO 14-1382 1R01HL128056-01A1 ( U.S. NIH Grant/Contract ) |
First Posted: | October 15, 2015 Key Record Dates |
Results First Posted: | April 20, 2020 |
Last Update Posted: | April 20, 2020 |
Last Verified: | April 2020 |
Atherosclerotic cardiovascular disease Inflammation reduction |
Cardiovascular Diseases Atherosclerosis Inflammation Pathologic Processes Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases Methotrexate Abortifacient Agents, Nonsteroidal Abortifacient Agents Reproductive Control Agents Physiological Effects of Drugs |
Antimetabolites, Antineoplastic Antimetabolites Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Dermatologic Agents Enzyme Inhibitors Folic Acid Antagonists Immunosuppressive Agents Immunologic Factors Antirheumatic Agents Nucleic Acid Synthesis Inhibitors |