Trials / Completed

CompletedNCT04865640

Clinical Validation Study for Noninvasive Cardiopulmonary Management Device

Clinical Validation Study for Noninvasive Cardiopulmonary Management Device.

Status: Completed
Phase: —
Study type: Observational
Enrollment: 40 (actual)

Sponsor: Analog Device, Inc. · Academic / Other
Sex: All
Age: 18 Years
Healthy volunteers: Accepted

Summary

The ADI At-Home CPM (Cardiopulmonary Management) System is a non-invasive device that measures and trends a variety of biological parameters. This study will be conducted as a prospective non-randomized study with two study arms/cohorts - one of healthy adult patients, one of pathologic patients who fit into the intended use population of the CPM System.

Conditions

Cardiopulmonary Disease

Interventions

Type	Name	Description
DIAGNOSTIC_TEST	Noninterventional and noninvasive	The ADI At-Home CPM (Cardiopulmonary Management) System is intended for adults undergoing monitoring for cardiopulmonary conditions under the direction of a licensed medical professional to measure, record, and periodically transmit physiological data.

Timeline

Start date: 2020-11-19
Primary completion: 2021-02-09
Completion: 2021-02-16
First posted: 2021-04-29
Last updated: 2024-08-06
Results posted: 2024-08-06

Locations

1 site across 1 country: United States

Regulatory

FDA-regulated device study

Source: ClinicalTrials.gov record NCT04865640. Inclusion in this directory is not an endorsement.