Monitor Patients With Sleep Apnea (ARMADA)

Corventis

Status: Completed

Conditions: Sleep Apnea

Treatments: Device: AVIVO system

Study type: Observational

Funder types: Industry

Identifiers

NCT00918502

COR-2009-004

Details and patient eligibility

About

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

Full description

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

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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