Skip to main content
OpenTrials
Completed

NCT Number: NCT00918502

Monitor Patients With Sleep Apnea

The primary objective of the study is to gather data to correlate physiological signals measured by the AVIVO™ Mobile Patient Management System with the patient's respiratory status, including apnea and hypopnea events, during polysomnography

Completed

Looking for future studies?

Notify Me

Key information

About this study

Patients with suspected sleep disordered breathing will be monitored during polysomnography and the collected information will be used to assess patient's respiratory status.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Is female or male, 18 years of age or older
  • Undergoing polysomnography for suspected sleep apnea
  • Is willing to provide written informed consent and comply with study guidelines

Treatment and study plan

Avivo System

Device

Non invasive external monitoring device

Sponsors and collaborators

Lead sponsor

Corventis, Inc.

Industry

Registry information

Official study title

Adherent Respiratory Monitoring for Apnea Detection and Evaluation Study

Acronym: ARMADA

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Jun 11, 2009
Registry last updated
Feb 4, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.