A Noninterventional, Single-Center Feasibility Study to Evaluate Measures of Heart Failure Risk
NCT05646056 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82
Last updated 2024-10-24
Summary
This is a non-invasive/observational study in healthy and mild HF subjects utilizing clinical and ambulatory measurements to improve detection, monitoring, and management of HF risks.
Conditions
- Heart Failure
- Cardiomyopathy, Hypertrophic
- Left Ventricular Hypertrophy
Interventions
- DEVICE
-
Software
Observation only
Sponsors & Collaborators
-
Prolaio
lead INDUSTRY
Principal Investigators
-
Michael Koren, MD · Jacksonville Center For Clinical Research
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-10-28
- Primary Completion
- 2024-09-18
- Completion
- 2024-09-18
- FDA Device
- Yes
Countries
- United States
Study Locations
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