Hypercapnic Respiratory Failure Clinical Trial
— TpCO2-NIVOfficial title:
Use of TpCO2 (Transcutaneous CO2 Measurement)as PaCO2 Predictor During Non Invasive Ventilation (NIV) in Case of Acute Hypercapnic Respiratory Failure
Verified date | June 2015 |
Source | University of Lausanne Hospitals |
Contact | n/a |
Is FDA regulated | No |
Health authority | Switzerland: Laws and standards |
Study type | Observational |
In patients suffering from hypercapnic respiratory failure and treated by non invasive ventilation (NIV), the interest of using transcutaneous CO2 measurement to evaluate PaCO2 and PaCO2 variation over time is unknown and will be evaluated in this study. Measurements will be done during one-hour NIV treatments.
Status | Completed |
Enrollment | 20 |
Est. completion date | March 2015 |
Est. primary completion date | March 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - ICU patient equipped with an arterial line - NIV treatment prescribed by the clinician in charge - Hypercapnia defined by PaCO2> 42mmHg Exclusion Criteria: - Severe hemodynamic instability - Severe psychiatric disorders - Denied consent - Age < 18 years |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Switzerland | Intensive care and burn unit, University hospital of Lausanne | Lausanne |
Lead Sponsor | Collaborator |
---|---|
University of Lausanne Hospitals |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Comparison between TpCO2 (transcutaneous non invasive CO2 partial pressure measurement) and PaCO2 (obtained by blood gas analysis) values during NIV treatment. | sixty minutes | No |
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