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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01997528
Other study ID # EK Nr. 1191/2013
Secondary ID
Status Recruiting
Phase N/A
First received November 7, 2013
Last updated November 22, 2013
Start date November 2013

Study information

Verified date November 2013
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority Austria: Austrian Medicines and Medical Devices Agency
Study type Interventional

Clinical Trial Summary

Oxygenatuion and decarboxylation during different settings (steps of blood flow and sweep gas flow) of extracorporeal gas exchange by ILA Activve using a jugular 22French double lumen cannula are measured.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria:

- Patient on ILA Activve

- Controlled mechanical ventilation

- No spontaneous breathing

Exclusion Criteria:

- Pregnancy

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Change of blood flow or sweep gas flow ( ILA Activve)


Locations

Country Name City State
Austria Dept. of Medicine I, ICU, General Hospital of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood gas analysis Changes after every 15 min. of each setting (13 settings leading to 195 min. altogether) No
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