Monitor Patients With Sleep Apnea

Adherent Respiratory Monitoring for Apnea Detection and Evaluation Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00918502

Acronym

ARMADA

Enrollment

Registered

2009-06-11

Start date

2009-03-31

Completion date

2009-07-31

Last updated

2010-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea

Brief summary

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

Detailed 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.

Interventions

DEVICEAVIVO system

Non invasive external monitoring device

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026