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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01319643
Other study ID # OXYGEN-TIPO-1.0-30-09-2009
Secondary ID 2009-016506-17
Status Recruiting
Phase Phase 4
First received August 30, 2010
Last updated March 21, 2011
Start date December 2009
Est. completion date November 2011

Study information

Verified date August 2010
Source University of Modena and Reggio Emilia
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

Oxygen administration is a common practice in intensive care units, although concern is growing about oxygen toxicity. The aim of the study is to access whether a rigorous maintenance of a state of normal oxygenation in critically ill patients could obtain better outcomes, such as mortality, infections and organ failures, in comparison to conventional oxygen therapy practice.


Recruitment information / eligibility

Status Recruiting
Enrollment 660
Est. completion date November 2011
Est. primary completion date November 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- all patients admitted in a post-operative and medical intensive care unit with expected admission of at least three days. Informed consensus as soon as possible

Exclusion Criteria:

- minority

- patient discharged from ICU and successively re-admitted

- patient enrolled in other studies

- expected survival shorter than 24 hours

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Intervention

Drug:
Oxygen
The lowest inspiratory fraction of oxygen between 21 and 100% in as a short time as possible to maintain SpO2 between 94 and 98% or PaO2 between 70 and 100 mmHg.

Locations

Country Name City State
Italy Terapia Intensiva Post-operatoria. Azienda Ospedaliero Universitaria Policlinico di Modena Modena

Sponsors (1)

Lead Sponsor Collaborator
University of Modena and Reggio Emilia

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality in ICU 30 days Yes
Secondary Rate of organ dysfunctions (respiratory, circulation, renal, liver) 30 days Yes
Secondary Rate of nosocomial blood and respiratory infections in intensive care unit and surgery site infections in hospital. 30 days Yes
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