NCT01455662

Brief Summary

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2010

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2010

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

September 28, 2011

Completed
22 days until next milestone

First Posted

Study publicly available on registry

October 20, 2011

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

November 3, 2011

Status Verified

November 1, 2011

Enrollment Period

1.9 years

First QC Date

September 28, 2011

Last Update Submit

November 2, 2011

Conditions

Cardiac Arrest

Keywords

cardiac arrest

Outcome Measures

Primary Outcomes (1)

  • mortality

    1 year

Secondary Outcomes (1)

  • correlation of clearance markers of perfusion with the use of vasopressor and positive fluid balance

    6 hours

Study Arms (1)

all patients after cardiac arrest

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients hospitalized in the intensive care unit after cardiopulmonary arrest

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Conceição Hospital

Porto Alegre, Rio Grande do Sul, Brazil

RECRUITING

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Vanessa Oliveira, MD

    Conceição Hospital

    PRINCIPAL INVESTIGATOR

  • Diego F Riveiro, MD

    Hospital Nossa Senhora da Conceição

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Vanessa M Oliveira, MD

CONTACT

05192513723vanessa.oliveira480@gmail.com

Diego Riveiro, MD

CONTACT

05184175632dmriveiro@yahoo.com.br

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 28, 2011

First Posted

October 20, 2011

Study Start

January 1, 2010

Primary Completion

December 1, 2011

Study Completion

December 1, 2011

Last Updated

November 3, 2011

Record last verified: 2011-11

Locations

BR(1)