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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01249794
Other study ID # GO/URC/ER/mm 183/DG
Secondary ID
Status Completed
Phase N/A
First received November 29, 2010
Last updated March 20, 2018
Start date September 2010
Est. completion date December 2013

Study information

Verified date March 2018
Source Università Vita-Salute San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with respiratory failure following cardiac surgery are randomized to receive standard therapy versus non invasive ventilation. The hypothesis is that patients receiving non invasive ventilation will perform better than those who received standard therapy.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- hypoxia

Exclusion Criteria:

- pneumothorax

- cardiocirculatory instability

- no written consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
non invasive ventilation
continuous positive airways pressure

Locations

Country Name City State
Italy Ospedale San Raffaele di Milano, Italy Milano

Sponsors (1)

Lead Sponsor Collaborator
Università Vita-Salute San Raffaele

Country where clinical trial is conducted

Italy, 

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