- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01455662
Relationship Between Tissue Markes in Patients With Post Cardio Respiratory Syndrome
Relationship Between Lactate and Venous Oxygen Saturation Gradient of Carbon Dioxide in Patients With Post Cardio Respiratory Syndrome
Study Overview
Status
Conditions
Detailed 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).
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Vanessa M Oliveira, MD
- Phone Number: 05192513723
- Email: vanessa.oliveira480@gmail.com
Study Contact Backup
- Name: Diego Riveiro, MD
- Phone Number: 05184175632
- Email: dmriveiro@yahoo.com.br
Study Locations
-
-
Rio Grande do Sul
-
Porto Alegre, Rio Grande do Sul, Brazil
- Recruiting
- Conceição Hospital
-
Principal Investigator:
- Vanessa Oliveira, MD
-
Principal Investigator:
- Diego Riveiro, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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 Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
all patients after cardiac arrest
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
mortality
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
correlation of clearance markers of perfusion with the use of vasopressor and positive fluid balance
Time Frame: 6 hours
|
6 hours
|
Collaborators and Investigators
Investigators
- Principal Investigator: Vanessa Oliveira, MD, Conceição Hospital
- Principal Investigator: Diego F Riveiro, MD, Hospital Nossa Senhora da Conceição
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10086
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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