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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03951779
Other study ID # 18-005354
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 14, 2018
Est. completion date January 10, 2020

Study information

Verified date March 2022
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Researchers are examining the diagnostic utility of an exercise cardiac MRI (eCMR) in the assessment of cardiac dyspnea (shortness of breath).


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date January 10, 2020
Est. primary completion date January 10, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Consecutive patients aged =18 years years with suspected cardiac dyspnea who are scheduled to undergo right heart catheterization as dictated by a comprehensive examination and echocardiography will be included for enrollment. Exclusion Criteria: - Age <18 years - Pregnancy - Mechanical ventilation - Acute or chronic renal failure (creatinine clearance <30 ml/min or requiring renal replacement therapy) - Inability to perform MRI (i.e. claustrophobia, severe obesity (>150 kg), device incompatible with MRI) - Inability to exercise - Significant arrhythmia that precludes adequate ECG-gating for the MRI (i.e. atrial fibrillation with highly variable cycle lengths) - Prior heart or lung transplantation - Left ventricular systolic (ejection fraction <50%) or diastolic failure (based on Framingham criteria for heart failure with preserved ejection fraction) - Significant left-sided valvular disease (=moderate aortic stenosis, mitral stenosis, aortic regurgitation, mitral regurgitation) or prior valve surgery

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Exercise cardiac magnetic resonance imaging
Subjects will exercise on a treadmill and immediately following the completion of the stress protocol, subjects will undergo cardiac magnetic resonance imaging

Locations

Country Name City State
United States Mayo Clinic in Florida Jacksonville Florida

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ejection Fraction Measured using exercise cardiac magnetic resonance imaging (eCMR) reported in percentages Baseline
Primary Stroke Volume Measured using exercise cardiac magnetic resonance imaging (eCMG) reported in mL Baseline
Primary Longitudinal Strain Assessment Measured using exercise cardiac magnetic resonance imaging (eCMG) reported in percentages Baseline
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