Avivo System
DeviceNon invasive external monitoring device
NCT Number: NCT00918502
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
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Notify Me18 year and older
All sexes
Observational
Patients with suspected sleep disordered breathing will be monitored during polysomnography and the collected information will be used to assess patient's respiratory status.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Non invasive external monitoring device
Corventis, Inc.
Industry
Adherent Respiratory Monitoring for Apnea Detection and Evaluation Study
Acronym: ARMADA
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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.
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