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Heart Failure Monitoring With a Portable Ultrasound Device With Artificial Intelligence Assisted Tools: A Multi-Phase Observational Feasibility Study

Heart Failure Monitoring With a Portable Ultrasound Device With Artificial Intelligence Assisted Tools: A Multi-Phase Observational Feasibility Study

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05594940
Enrollment
22
Registered
2022-10-26
Start date
2022-09-21
Completion date
2024-02-23
Last updated
2024-02-26

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

Conditions

Congestive Heart Failure

Keywords

CardioMEMS, iQ+, Home, CHF, B-Lines

Brief summary

The primary objective of this study is to evaluate the feasibility of a novel app to facilitate heart failure patients to acquire lung ultrasound images and evaluate the quality of those images to expert scans, and to evaluate for relationships between the ultrasound data and pulmonary pressure data from the Abbott CardioMEMS system.

Detailed description

Feasibility study to compare an investigational Artificial Intelligence (AI) Auto B-line tool measurement on Lung Ultrasound (US) images acquired with an AI assisted guidance tool by novice ultrasound clinicians and heart failure (HF) patients, to standard of care heart failure monitoring of pulmonary artery pressure measured by the Abbott CardioMEMS system.

Interventions

None listed

Sponsors

Butterfly Network
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Documented diagnosis of heart failure at least three months prior to the date of consent 2. HF currently managed with the Abbott CardioMEMS device 3. Able to read and write in English. 4. At least 18 years of age or older on the date of consent. 5. Willing and able to provide written consent to participation 6. Expressed willingness to capture AI assisted US recordings immediately before or after taking their CardioMEMS measurements 7. Access to WiFi or cellular data connection at home 8. In the opinion of the investigator or delegate the subject, must be capable of complying with study procedures.

Exclusion criteria

1. Previous experience using an ultrasound device on themselves or others 2. Women who are pregnant or plan to become pregnant during the study

Design outcomes

Primary

MeasureTime frameDescription
Patients Image QualityStudy Completion (91 days)Image quality comparisons between ultrasound scans performed by heart failure patients using the study app to traditional ultrasound scans performed by trained clinicians
Novice Image QualityStudy Completion (91 days)Image quality comparisons between ultrasound scans performed by novice clinicians using the study app to traditional ultrasound scans performed by trained clinicians
B-Line count CardioMEMS comparisonStudy Completion (91 days)Relationship comparisons between ultrasound data from exams performed by heart failure patients using the study app (both in clinic and at home) and ultrasound exams performed by novice clinicians to pulmonary pressure data from the Abbott CardioMEMS system

Secondary

MeasureTime frameDescription
Ease of useStudy Completion (91 days)Patient and novice clinician reported ease of use and satisfaction based on responses to user surveys.

Countries

United States

Outcome results

None listed

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