Use of TpCO2 (Transcutaneous CO2 Measurement) as PaCO2 Predictor During NIV in Case of Acute Hypercapnic Respiratory Failure

NCT ID: NCT01857635

Last Updated: 2015-06-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-02-28

Study Completion Date

2015-03-31

Brief Summary

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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.

Detailed Description

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Conditions

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Hypercapnic Respiratory Failure

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Lausanne Hospitals

OTHER

Sponsor Role lead

Responsible Party

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Prof. Philippe Jolliet

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Philippe Jolliet, Prof

Role: PRINCIPAL_INVESTIGATOR

University of Lausanne Hospitals

Locations

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Intensive care and burn unit, University hospital of Lausanne

Lausanne, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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TpCO2-NIV

Identifier Type: -

Identifier Source: org_study_id

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