About this trial
The researchers are doing this study to see how well cardiac magnetic resonance imaging (CMR) scans can be used to examine the properties of central venous catheter-associated right atrial clot (RA clot). This could help doctors decide on the best treatment options.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Documentation of Disease
Definition of Disease [or Measurable Disease]
Cardiac mass (CMASS) will be initially localized on cine-CMR, on which it is defined via established criteria as a discrete tissue prominence independent from normal anatomic structures, quantified based on size (area, cross-sectional linear dimensions)
CMASS will be further categorized by type (CNEO or CTHR) based on CMR tissue characterization: CNEO and CTHR can be differentiated based on presence of contrast enhancement via the reference standard of LGE-CMR using established criteria previously validated by our group and others.
Disqualifiers
Known pre-existing CV disease which can affect hemodynamics within cardiac chambers as determined by the investigator, including
Arrhythmia - chronic persistent atrial arrhythmias
Cardiomyopathies including Ischemic or non-ischemic cardiomyopathy with LVEF <53%
Restrictive cardiomyopathy - cardiac amyloidosis, myocardial fibrosis
Trial design
Single group
Treatments tested in this trial
Cardiac MRI
Diagnostic testCardiac MRI (CMR) for Central venous catheter-associated right atrial thrombus (RATHR) patients will be performed at baseline within 1 month of suspected RATHR diagnosis on echo/chest CT, and a follow up (3 months)
Treatment groups
Trial outcomes
Primary outcomes
association between Central venous catheter-associated right atrial thrombus (RATHR) with Cardiac MRI (CMR) tissue
Quantitative tissue characterization of RATHR will be employed to measure RATHR organization based on contrast infiltration, T1 variability altered T2\*10 and susceptibility. These will be used to determine chronicity of thrombi as a predictor of therapeutic response to anticoagulation. Analyses will also include assessment of RATHR size, and geometry (border irregularity) at baseline and at 3-month follow up CMR using established methods to assess for the degree of resolution of RATHR.
Sponsors and contacts
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Memorial Sloan Kettering Cancer Center
Lead sponsor
American Heart Association
Collaborator