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Post Market, Prospective Multicenter Observational Study of the Safety and Performance of Bellavista Ventilator

NCT05383651 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2024-09-05

No results posted yet for this study

Summary

This prospective post market clinical follow up (PMCF) study will evaluate the safety and performance of bellavista ventilator and the iFlow sensors in daily clinical routine.

Conditions

  • Ventilation Therapy; Complications

Interventions

DEVICE

bellavista 1000

observational use of Bellavista 1000 ventilator in adult ventilated patients

DEVICE

bellavista 1000 neo

observational use of Bellavista 1000 ventilator in neonatal ventilated patients

Sponsors & Collaborators

  • Vyaire Medical

    lead INDUSTRY

Eligibility

Min Age
6 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2024-05-31
Completion
2024-06-30

Countries

  • Canada
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05383651 on ClinicalTrials.gov