RECRUITING

Automated Ultrasound Cardiac Guidance Tool

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed

Official Title

Optimization of an Ultrasound Cardiac Guidance Tool

Quick Facts

Study Start:2023-02-01

Study Completion:2027-05-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05649826

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 120 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Males and females, aged 18 years and older 2. Subject willing and able to give written informed consent	1. Emergency (non-elective) admission within 24 h prior to participating in the study 2. Female subjects who are pregnant (women of childbearing potential will provide a statement that they are not pregnant incorporated in the ICF 3. Unable to lie as required in all the classic positions for standard TTE exam: supine on back / left decubitus 4. Subjects who currently participate in a clinical trial, involving interventional cardiac devices. 5. Subjects who have prior Echo exam with description of Low/Poor quality exam in the echo report. 6. Subjects with BMI above 40. 7. Subjects experiencing a known or suspected acute cardiac event. 8. Subjects with severe chest wall deformity as per previous medical records and physical examination. 9. Subjects who have undergone pneumonectomy. 10. Subjects whose anatomy does not lend itself to yield diagnosable standard echocardiography clips (i.e., situs inversus with dextrocardia, single ventricle anatomy due to congenital heart disease, etc.).

Inclusion Criteria

Exclusion Criteria

1. Males and females, aged 18 years and older
2. Subject willing and able to give written informed consent

1. Emergency (non-elective) admission within 24 h prior to participating in the study
2. Female subjects who are pregnant (women of childbearing potential will provide a statement that they are not pregnant incorporated in the ICF
3. Unable to lie as required in all the classic positions for standard TTE exam: supine on back / left decubitus
4. Subjects who currently participate in a clinical trial, involving interventional cardiac devices.
5. Subjects who have prior Echo exam with description of Low/Poor quality exam in the echo report.
6. Subjects with BMI above 40.
7. Subjects experiencing a known or suspected acute cardiac event.
8. Subjects with severe chest wall deformity as per previous medical records and physical examination.
9. Subjects who have undergone pneumonectomy.
10. Subjects whose anatomy does not lend itself to yield diagnosable standard echocardiography clips (i.e., situs inversus with dextrocardia, single ventricle anatomy due to congenital heart disease, etc.).

Contacts and Locations

Study Contact

Robert Ehrman, MD

CONTACT

313-5771268

rehrman@med.wayne.edu

Laura Gowland, Sonographer

CONTACT

313-5771268

lgowland@med.wayne.edu

Principal Investigator

Robert Ehrman, MD

PRINCIPAL_INVESTIGATOR

Wayne University Emergency medicine

Noa Avisar, PhD

STUDY_DIRECTOR

UltraSight

Study Locations (Sites)

Wayne University

Detroit, Michigan, 48201

United States

Collaborators and Investigators

Sponsor: UltraSight

Robert Ehrman, MD, PRINCIPAL_INVESTIGATOR, Wayne University Emergency medicine
Noa Avisar, PhD, STUDY_DIRECTOR, UltraSight

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-02-01

Study Completion Date2027-05-01

Study Record Updates

Study Start Date2023-02-01

Study Completion Date2027-05-01

Terms related to this study

Additional Relevant MeSH Terms

Ultrasound Imaging