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Cardiac Autonomic Function For Risk Stratification in the Emergency Room (PREDICT-ER)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Axel Bauer, University Hospital Tuebingen
ClinicalTrials.gov Identifier:
NCT01486589
First received: December 2, 2011
Last updated: February 5, 2014
Last verified: February 2014
December 2, 2011
February 5, 2014
October 2010
June 2013   (Final data collection date for primary outcome measure)
In-hospital mortality [ Time Frame: 10 days ]
In-hospital mortality [ Time Frame: 30 days ]
Complete list of historical versions of study NCT01486589 on ClinicalTrials.gov Archive Site
  • Cardiac mortality [ Time Frame: 10 days ]
  • transfer to intensive care unit [ Time Frame: 10 days ]
  • hospital discharge [ Time Frame: 48 hours ]
  • duration of hospital stay [ Time Frame: within 30 days ]
  • costs of health care [ Time Frame: 30 days ]
  • 180 day mortality [ Time Frame: 180 days ]
  • Cardiac mortality [ Time Frame: 30 days ]
  • transfer to intensive care unit [ Time Frame: 30 days ]
  • hospital discharge [ Time Frame: 48 hours ]
  • duration of hospital stay [ Time Frame: within 30 days ]
  • costs of health care [ Time Frame: 30 days ]
Not Provided
Not Provided
 
Cardiac Autonomic Function For Risk Stratification in the Emergency Room
Risk Stratification in the Emergency Room by Cardiac Autonomic Function
The aim of the study is to test the hypothesis that impaired cardiac autonomic function predicts adverse outcome in unselected patients presenting in the emergency ward.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample
Consecutive patients presenting at the emergency department of the University Hospital of Tübingen
Autonomic Nervous System Activity
Not Provided
Not Provided
Eick C, Rizas KD, Meyer-Zürn CS, Groga-Bada P, Hamm W, Kreth F, Overkamp D, Weyrich P, Gawaz M, Bauer A. Autonomic nervous system activity as risk predictor in the medical emergency department: a prospective cohort study. Crit Care Med. 2015 May;43(5):1079-86. doi: 10.1097/CCM.0000000000000922.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
6521
Not Provided
June 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

- presenting at the emergency department of the University Hospital of Tübingen

Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
 
NCT01486589
577/2011BO1
No
Not Provided
Not Provided
Axel Bauer, University Hospital Tuebingen
Thebiosignals.com
Not Provided
Not Provided
Thebiosignals.com
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP