MedTrace Logo

Monitoring of Non-invasive Ventilation

NCT01845233 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 67

Last updated 2014-08-25

No results posted yet for this study

Summary

The purpose of this study is to determine whether clinical examination, report from ventilator software, nocturnal Sp02 and daytime arterial blood gas are sufficient as screening tools to reveal clinical relevant problems with patients receiving long term treatment with non invasive ventilation.

Conditions

  • Hypoventilation

Sponsors & Collaborators

  • Haukeland University Hospital

    collaborator OTHER

  • Trondheim University Hospital

    collaborator OTHER

  • University Hospital, Geneva

    collaborator OTHER

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Sigurd aarrestad, MD · Oslo University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • Norway

Study Locations

More Related Trials

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 NCT01845233 on ClinicalTrials.gov