Monitoring of Non-invasive Ventilation
Completed
- Conditions
- Hypoventilation
- Registration Number
- NCT01845233
- Lead Sponsor
- Oslo University Hospital
- Brief 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.
- Detailed Description
Patient with chronic hypoventilation with stable on long term treatment (LTMV) with non-invasive ventilation for at least 3 month taking part of our LTMV program will be included.
In addition to clinical examination,report from ventilator software, nocturnal Sp02 and daytime arterial blood gas all patients will be investigated with sleep polygraphy and transcutaneous Co2.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 67
Inclusion Criteria
Not provided
Exclusion Criteria
- Under 18 years old
- Lack of cooperation
- Pregnant
- Acute exacerbation last 3 month leading to hospital admission.
- Change of treatment last 3 month
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of transcutaneous co2 revealing sleep hypoventilation, when nocturnal pulseoximeter is normal single night study
- Secondary Outcome Measures
Name Time Method Frequency of patient-ventilator asynchrony during non invasive ventilation ? Single night study
Trial Locations
- Locations (1)
Oslo University Hospital
🇳🇴Oslo, Norway