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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01455662
Other study ID # 10086
Secondary ID
Status Recruiting
Phase N/A
First received September 28, 2011
Last updated November 2, 2011
Start date January 2010
Est. completion date December 2011

Study information

Verified date November 2011
Source Hospital Nossa Senhora da Conceicao
Contact Vanessa M Oliveira, MD
Phone 05192513723
Email vanessa.oliveira480@gmail.com
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Observational

Clinical Trial Summary

There is a correlation between hospital mortality and changes in markers of tissue perfusion, lactate, and venous oxygen saturation and carbon dioxide gradient.


Description:

Evaluation of the serum carbon dioxide gradient (GapCO2), central venous saturation (ScvO2) and the clearance of serum lactate (Clac) in predicting hospital mortality after cardiac arrest syndrome (post-PCR).

Prospective study, unicenter - Intensive Care Unit - HNSC. Period: May/2010 to June/2011. Serial assessment of GapCO2 of ScvO2 Clac and the first 72 hours post-PCR. Excluded under 18, survival of less than 6HS, pregnant women, traumatized, post-operative hypothermia and liver disease. T-student test, 95% (p <0.05).


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- All patients hospitalized in the intensive care unit after cardiopulmonary arrest with any pace

Exclusion Criteria:

pregnant women, traumatized, post-operative(less 7 days), hypothermia and liver disease.

- patients hospitalized in the intensive care unit with more than 6 hours post cardiac arrest

- less 18 years old

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil Conceição Hospital Porto Alegre Rio Grande do Sul

Sponsors (1)

Lead Sponsor Collaborator
Hospital Nossa Senhora da Conceicao

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality 1 year Yes
Secondary correlation of clearance markers of perfusion with the use of vasopressor and positive fluid balance 6 hours Yes
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