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DEF-315 Better Accuracy in Ejection Fraction (EF) Assessment With DEFINITY

A Phase III, Open-Label, Multicenter Trial to Evaluate Ejection Fraction, End-Diastolic and End-Systolic Volumes, by Unenhanced and DEFINITY®-Enhanced 2D-Echo and Magnetic Resonance Imaging

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03719612
Acronym
BENEFIT2
Enrollment
160
Registered
2018-10-25
Start date
2018-12-28
Completion date
2020-01-09
Last updated
2021-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Disease

Keywords

Left Ventricular Ejection Fraction, DEFINITY®, Enhanced Echocardiogram, Cardiac Magnetic Resonance

Brief summary

This is a Phase 3, prospective, open-label, multicenter study to evaluate Left Ventricular Ejection Fraction (LVEF) measurement accuracy and reproducibility of DEFINITY® contrast-enhanced and unenhanced echocardiography as compared with non-contrast cardiac magnetic resonance imaging (CMR) used as the truth standard.

Interventions

All subjects will receive a single dose of DEFINITY®

Sponsors

Syneos Health
CollaboratorOTHER
Lantheus Medical Imaging
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Men and women ≥ 18 years of age in sinus rhythm 2. Able to communicate effectively with trial personnel 3. LVEF measurements obtained via 2D Echo with or without contrast obtained within 6 months prior to enrollment (Day 0) 4. Has provided signed informed consent after receiving a verbal and written explanation of this clinical trial

Exclusion criteria

1. Female subjects who are pregnant or lactating. All women of child bearing potential \[WOCBP\] must have a negative urine pregnancy test at screening regardless of contraceptive use history. 2. Women of child-bearing potential are excluded unless they: 1. are post-menopausal defined as amenorrhea ≥ 12 consecutive months, OR 2. have undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation or bilateral oophorectomy), OR 3. have been using an adequate and medically approved method of contraception to avoid pregnancy for at least 1 month prior to DEFINITY® dose administration and be willing to continue using the same method for the duration of the study. 3. Current illness or pathology that would prevent undergoing investigational product administration due to a significant safety risk to the patient. 4. Uncontrolled arterial hypertension (defined as systolic blood pressure ≥ 200 mmHg or diastolic blood pressure ≥ 110 mmHg) or arterial hypotension (defined as systolic blood pressure ≤ 90 mmHg). 5. Unstable cardiovascular status defined as: 1. myocardial infarction or unstable angina pectoris within 6 months prior to enrollment/DEFINITY® dose administration day 2. transient ischemic attack or stroke within 3 months prior to DEFINITY® dose administration 3. symptomatic valvular heart disease or moderate to severe stenotic valvular heart disease 4. clinically significant congenital heart defects 5. current uncontrolled cardiac arrhythmias causing symptoms or hemodynamic compromise 6. acute pulmonary embolus or pulmonary infarction 7. acute myocarditis or pericarditis 8. acute aortic dissection 9. atrial fibrillation 6. any major surgery within 4 weeks prior to screening 7. known contraindications to undergoing CMR (e.g. implanted pacemakers, cardioverter, defibrillators) or claustrophobia 8. participation in any investigational drug, device, or placebo study within 30 days prior to screening 9. known hypersensitivity to perflutren, or any of the excipients in DEFINITY® 10. prisoners or those who are subject to compulsory detention or involuntary incarceration for treatment of either a psychiatric or physical illness (e.g., infectious disease).

Design outcomes

Primary

MeasureTime frameDescription
Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderUp to 30 days between day of echocardiograms and CMR imagingDemonstrate improvement in accuracy in left ventricular ejection fraction (LVEF) assessment using DEFINITY® contrast-enhanced over unenhanced echocardiography by comparing LVEF percentage differences from CMR measured by 3 independent blinded image readers.

Secondary

MeasureTime frameDescription
Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsUp to 30 days between day of echocardiogram and CMR imagingDemonstrate improvement in accuracy in left ventricular ejection fraction (LVEF) assessment using DEFINITY® contrast-enhanced over unenhanced echocardiography in subjects with suboptimal echocardiograms by comparing LVEF percentage differences from CMR measured by 3 independent blinded readers.
Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersUp to 30 days between day of echocardiograms and CMR imagingDemonstrate a reduction in inter-reader variability for the assessment of left ventricular ejection fraction using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing LVEF percentage differences from CMR between 3 independent blinded readers.
Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersUp to 30 days between day of echocardiogram and CMR imagingDemonstrate a reduction in inter-reader variability for the assessment of end-diastolic/systolic volumes using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing end-diastolic and systolic volume differences from CMR between 3 independent blinded readers.
Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsUp to 30 days between day of echocardiograms and CMR imagingDemonstrate a reduction in inter-reader variability for the assessment of left ventricular ejection fraction using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing LVEF percentage differences from CMR between 3 independent blinded readers in subjects with suboptimal echocardiograms.
Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsUp to 30 days between day of echocardiograms and CMR imagingDemonstrate a reduction in inter-reader variability for the assessment of end-diastolic/systolic volumes using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing end-diastolic and systolic volume differences from CMR between 3 independent blinded readers in subjects with suboptimal echocardiograms.

Countries

United States

Participant flow

Participants by arm

ArmCount
DEFINITY®
Each patient will undergo an unenhanced ultrasound examination and a DEFINITY® contrast-enhanced ultrasound DEFINITY®: All subjects will receive a single dose of DEFINITY®
160
Total160

Baseline characteristics

CharacteristicDEFINITY®
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
54 Participants
Age, Categorical
Between 18 and 65 years
106 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
14 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
146 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
LVEF Group
LVEF <30%
45 Participants
LVEF Group
LVEF 30-40%
48 Participants
LVEF Group
LVEF 41-50%
27 Participants
LVEF Group
LVEF >50%
40 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
3 Participants
Race (NIH/OMB)
Black or African American
32 Participants
Race (NIH/OMB)
More than one race
2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
2 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
120 Participants
Sex: Female, Male
Female
55 Participants
Sex: Female, Male
Male
105 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 160
other
Total, other adverse events
0 / 160
serious
Total, serious adverse events
1 / 160

Outcome results

Primary

Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader

Demonstrate improvement in accuracy in left ventricular ejection fraction (LVEF) assessment using DEFINITY® contrast-enhanced over unenhanced echocardiography by comparing LVEF percentage differences from CMR measured by 3 independent blinded image readers.

Time frame: Up to 30 days between day of echocardiograms and CMR imaging

Population: Modified ITT Population

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Enhanced5.70 Percent Ejection FractionStandard Deviation 4.292
Blinded Reader 1Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Unenhanced6.08 Percent Ejection FractionStandard Deviation 4.53
Blinded Reader 2Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Unenhanced6.00 Percent Ejection FractionStandard Deviation 4.813
Blinded Reader 2Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Enhanced5.88 Percent Ejection FractionStandard Deviation 4.33
Blinded Reader 3Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Enhanced5.03 Percent Ejection FractionStandard Deviation 3.548
Blinded Reader 3Absolute Value of LVEF Percentage Differences From CMR by Blinded ReaderEcho Unenhanced5.36 Percent Ejection FractionStandard Deviation 3.889
p-value: 0.358t-test, 2 sided
p-value: 0.804t-test, 2 sided
p-value: 0.371t-test, 2 sided
Secondary

Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal Echocardiograms

Demonstrate improvement in accuracy in left ventricular ejection fraction (LVEF) assessment using DEFINITY® contrast-enhanced over unenhanced echocardiography in subjects with suboptimal echocardiograms by comparing LVEF percentage differences from CMR measured by 3 independent blinded readers.

Time frame: Up to 30 days between day of echocardiogram and CMR imaging

Population: Modified ITT Population - Sub-optimal Echocardiograms

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Enhanced5.67 Percent Ejection FractionStandard Deviation 3.717
Blinded Reader 1Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Unenhanced6.95 Percent Ejection FractionStandard Deviation 5.219
Blinded Reader 2Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Enhanced6.16 Percent Ejection FractionStandard Deviation 3.746
Blinded Reader 2Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Unenhanced6.81 Percent Ejection FractionStandard Deviation 4.694
Blinded Reader 3Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Enhanced4.68 Percent Ejection FractionStandard Deviation 3.456
Blinded Reader 3Secondary Objective 1: Absolute Value of LVEF Percentage Differences From CMR by Blinded Reader for Sub-optimal EchocardiogramsEcho Unenhanced5.33 Percent Ejection FractionStandard Deviation 3.764
p-value: 0.03t-test, 2 sided
p-value: 0.312t-test, 2 sided
p-value: 0.347t-test, 2 sided
Secondary

Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded Readers

Demonstrate a reduction in inter-reader variability for the assessment of left ventricular ejection fraction using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing LVEF percentage differences from CMR between 3 independent blinded readers.

Time frame: Up to 30 days between day of echocardiograms and CMR imaging

Population: Modified ITT Population

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Enhanced5.70 Percent Ejection FractionStandard Deviation 4.292
Blinded Reader 1Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Unenhanced6.08 Percent Ejection FractionStandard Deviation 4.53
Blinded Reader 2Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Enhanced5.88 Percent Ejection FractionStandard Deviation 4.33
Blinded Reader 2Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Unenhanced6.00 Percent Ejection FractionStandard Deviation 4.813
Blinded Reader 3Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Enhanced5.03 Percent Ejection FractionStandard Deviation 3.548
Blinded Reader 3Secondary Objective 2: Absolute Value LVEF Percentage Differences From CMR Between Blinded ReadersEcho Unenhanced5.36 Percent Ejection FractionStandard Deviation 3.889
Comparison: Inter-Reader Variability Echo Enhanced95% CI: [0.977, 0.988]
Comparison: Inter-Reader Variability Echo Unenhanced95% CI: [0.936, 0.966]
Comparison: Inter-Reader Variability Echo Enhanced95% CI: [0.958, 0.978]
Comparison: Inter-Reader Variability Echo Unenhanced95% CI: [0.923, 0.959]
Comparison: Inter-Reader Variability Echo Enhanced95% CI: [0.947, 0.972]
Comparison: Inter-Reader Variability Echo Unenhanced95% CI: [0.92, 0.958]
Secondary

Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers

Demonstrate a reduction in inter-reader variability for the assessment of end-diastolic/systolic volumes using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing end-diastolic and systolic volume differences from CMR between 3 independent blinded readers.

Time frame: Up to 30 days between day of echocardiogram and CMR imaging

Population: Modified ITT Population

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Diastolic57.85 mLStandard Deviation 44.204
Blinded Reader 1Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Diastolic64.91 mLStandard Deviation 44.084
Blinded Reader 1Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Systolic38.05 mLStandard Deviation 32.921
Blinded Reader 1Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Systolic42.87 mLStandard Deviation 34.793
Blinded Reader 2Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Systolic39.08 mLStandard Deviation 34.139
Blinded Reader 2Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Diastolic51.13 mLStandard Deviation 43.391
Blinded Reader 2Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Systolic32.41 mLStandard Deviation 32.896
Blinded Reader 2Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Diastolic62.01 mLStandard Deviation 43.392
Blinded Reader 3Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Systolic32.45 mLStandard Deviation 31.314
Blinded Reader 3Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Unenhanced End Diastolic48.32 mLStandard Deviation 39.895
Blinded Reader 3Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Systolic31.68 mLStandard Deviation 30.603
Blinded Reader 3Secondary Objective 3: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded ReadersEcho Enhanced End Diastolic47.97 mLStandard Deviation 40.589
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced95% CI: [0.978, 0.988]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced95% CI: [0.967, 0.983]
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced95% CI: [0.963, 0.981]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced95% CI: [0.91, 0.952]
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced95% CI: [0.962, 0.98]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced95% CI: [0.896, 0.945]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced95% CI: [0.984, 0.992]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced95% CI: [0.977, 0.988]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced95% CI: [0.978, 0.989]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced95% CI: [0.928, 0.962]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced95% CI: [0.969, 0.984]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced95% CI: [0.92, 0.958]
Secondary

Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal Echocardiograms

Demonstrate a reduction in inter-reader variability for the assessment of left ventricular ejection fraction using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing LVEF percentage differences from CMR between 3 independent blinded readers in subjects with suboptimal echocardiograms.

Time frame: Up to 30 days between day of echocardiograms and CMR imaging

Population: Modified ITT Population - Sub-optimal Echocardiograms

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Enhanced5.67 Percent Ejection FractionStandard Deviation 3.717
Blinded Reader 1Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Unenhanced6.95 Percent Ejection FractionStandard Deviation 5.219
Blinded Reader 2Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Enhanced6.16 Percent Ejection FractionStandard Deviation 3.746
Blinded Reader 2Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Unenhanced6.81 Percent Ejection FractionStandard Deviation 4.694
Blinded Reader 3Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Enhanced4.68 Percent Ejection FractionStandard Deviation 3.456
Blinded Reader 3Secondary Objective 4: Absolute Value of LVEF Percentage Differences From CMR Between Readers for Sub-optimal EchocardiogramsEcho Unenhanced5.33 Percent Ejection FractionStandard Deviation 3.764
Comparison: Inter-Reader Variability Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.956, 0.986]
Comparison: Inter-Reader Variability Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.888, 0.963]
Comparison: Inter-Reader Variability Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.931, 0.978]
Comparison: Inter-Reader Variability Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.864, 0.955]
Comparison: Inter-Reader Variability Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.907, 0.97]
Comparison: Inter-Reader Variability Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.834, 0.945]
Secondary

Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal Echocardiograms

Demonstrate a reduction in inter-reader variability for the assessment of end-diastolic/systolic volumes using DEFINITY® contrast-enhanced versus unenhanced echocardiography by comparing end-diastolic and systolic volume differences from CMR between 3 independent blinded readers in subjects with suboptimal echocardiograms.

Time frame: Up to 30 days between day of echocardiograms and CMR imaging

Population: Modified ITT Population - Sub-optimal Echocardiograms

ArmMeasureGroupValue (MEAN)Dispersion
Blinded Reader 1Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Diastolic71.67 mLStandard Deviation 49.916
Blinded Reader 1Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Diastolic74.89 mLStandard Deviation 51.468
Blinded Reader 1Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Systolic45.59 mLStandard Deviation 32.844
Blinded Reader 1Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Systolic48.00 mLStandard Deviation 37.639
Blinded Reader 2Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Systolic41.88 mLStandard Deviation 32.989
Blinded Reader 2Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Diastolic63.73 mLStandard Deviation 49.571
Blinded Reader 2Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Systolic38.55 mLStandard Deviation 33.493
Blinded Reader 2Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Diastolic69.07 mLStandard Deviation 46.316
Blinded Reader 3Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Systolic40.72 mLStandard Deviation 32.333
Blinded Reader 3Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Unenhanced End Diastolic64.38 mLStandard Deviation 46.827
Blinded Reader 3Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Systolic39.52 mLStandard Deviation 30.946
Blinded Reader 3Secondary Objective 5: Absolute Value End-diastolic and Systolic Volume Differences From CMR Between Blinded Readers for Suboptimal EchocardiogramsEcho Enhanced End Diastolic61.86 mLStandard Deviation 47.523
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.971, 0.991]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.956, 0.986]
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.959, 0.987]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.896, 0.966]
Comparison: Inter-Reader Variability End Diastolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.959, 0.987]
Comparison: Inter-Reader Variability End Diastolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.866, 0.956]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.982, 0.994]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.957, 0.986]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.973, 0.991]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.876, 0.959]
Comparison: Inter-Reader Variability End Systolic Echo Enhanced Sub-Optimal Echocardiograms95% CI: [0.966, 0.989]
Comparison: Inter-Reader Variability End Systolic Echo Unenhanced Sub-Optimal Echocardiograms95% CI: [0.855, 0.952]

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026