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Kosmos Trio and Ejection Fraction Pivotal Study

Kosmos Trio and Ejection Fraction Pivotal Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06027164
Enrollment
153
Registered
2023-09-07
Start date
2023-08-04
Completion date
2024-05-16
Last updated
2024-05-21

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

Conditions

Cardiac Disease

Brief summary

This is a single-group, observational study which will involve obtaining two echo scans of recruited patients. All recruited patients will undergo echo scans by both novice users (nurses) and experts (echo sonographers). Image quality between novices and experts as well as the ability to calculate LVEF from novice and expert scans and the quality of the LVEF calculated via KOSMOS-EF compared to LVEF calculations by expert cardiologists will occur in post-hoc Echo image analysis

Interventions

DEVICEPortable Ultrasound System

EchoNous KOSMOS

Sponsors

University of California, San Francisco
CollaboratorOTHER
Revival Research Institute LLC
CollaboratorUNKNOWN
Centaur Labs
CollaboratorUNKNOWN
EchoNous Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18-89 years of age * Have capacity to provide written consent either themselves or via healthcare proxy as determined by subjects' clinical care teams * Have an anticipated timeline in the EDOU long enough to allow for completion of study procedures without causing delay to subjects' usual clinical care

Exclusion criteria

* Heart rate \> 110 beats per minute at the time of recruitment * Pregnant women * Prior chest surgery * Chest wall deformities or injuries (i.e. wounds, infections, etc) * Limited mobility precluding them from turning in bed independently * Speak a primary language other than English or Spanish * Vulnerable populations including: patients being evaluated for psychiatric crises, incarcerated individuals * Unwilling or unable to consent to study procedures

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Global Left Ventricular FunctionUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if a study exam acquired by a nurses is of sufficient image quality to make a qualitative visual assessment of the Global Left Ventricular Function.
Assessment of Left Ventricular SizeUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if a study exam acquired by a nurse is of sufficient image quality to make a qualitative visual assessment of the Left Ventricular Size.
Assessment of Non-Trivial Pericardial EffusionUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if a study exam acquired by a nurse is of sufficient image quality to make a qualitative visual assessment of Non-Trivial Pericardial Effusion.
Assessment of Right Ventricular SizeUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if a study exam acquired by a nurse is of sufficient image quality to make a qualitative visual assessment of Right Ventricle Size.

Secondary

MeasureTime frameDescription
Manual vs. KOSMOS-EF for Sonographer ScansUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsMeasurements are computed for A4C and A2C scans acquired by sonographers . We will compare KOSMOS-EF LVEF calculation to LVEF calculated by a panel of cardiologists via a majority vote.
Assessment of Left Atrial SizeUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if a study exam acquired by a nurse is of sufficient image quality to make a qualitative visual assessment of Left Atrial Size.
Assessment of Automatic Structure LabellingUp to 2 months from the completion of the study or when all expert cardiologists readers independently complete their assessmentsA panel of cardiologists will access and determine via a majority vote if the frame-level false discovery rate (FDR) of automated cardiac structure labeling as determined by expert cardiologists for scans acquired by cardiac sonographers.

Countries

United States

Outcome results

None listed

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