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OpenTrials
Completed

NCT Number: NCT01486589

Cardiac Autonomic Function For Risk Stratification in the Emergency Room

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.

Completed

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Key information

Conditions

Autonomic Nervous System Activity

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Medizinische Universitätsklinik Tübingen

Tübingen, Baden-Wurttemberg, 72076, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Treatment and study plan

Primary outcomes

  1. In-hospital mortality

    Time frame: 10 days

Secondary outcomes

  1. Cardiac mortality

    Time frame: 10 days

  2. transfer to intensive care unit

    Time frame: 10 days

  3. hospital discharge

    Time frame: 48 hours

  4. duration of hospital stay

    Time frame: within 30 days

  5. costs of health care

    Time frame: 30 days

  6. 180 day mortality

    Time frame: 180 days

Sponsors and collaborators

Lead sponsor

Thebiosignals.com

Other

Registry information

Official study title

Risk Stratification in the Emergency Room by Cardiac Autonomic Function

Acronym: PREDICT-ER

Important dates

Study start
2010
Primary completion
2013
First posted
Dec 6, 2011
Registry last updated
Feb 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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