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OpenTrials
Completed

NCT Number: NCT00449969

Out-of-hospital Cardiopulmonary Resuscitation and AED Feedback

The purpose of this study is to determine whether an online automatic feedback improved CPR quality (No-flow time, compression depth, short-term survival and one year follow up) in this prospective randomised study of out-of-hospital cardiac arrest

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Anesthesiology and Intensive Care, University Hospital Muenster

Münster, D-48149, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • cardiac arrest

Exclusion criteria

  • age under 18 years

Treatment and study plan

Zoll AED pro

Device

Arm one (Extended feedback) offers full feedback guidance during CPR

Primary outcomes

  1. ratio of patients with spontaneous circulation

    Time frame: admission to the hospital

Secondary outcomes

  1. length of hospital stay

    Time frame: hospital discharge

  2. neurological status

    Time frame: hospital discharge

  3. neurological status

    Time frame: one year after resuscitation

Sponsors and collaborators

Lead sponsor

University Hospital Muenster

Other

Registry information

Official study title

Quality of Out-of-hospital Cardiopulmonary Resuscitation (CPR) With Real Time Automated Feedback: a Prospective Randomized Study

Important dates

Study start
2007
Primary completion
2009
Study completion
2010
First posted
Mar 21, 2007
Registry last updated
Apr 22, 2011

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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