Assessing CPR Quality During In-Hospital Cardiac Arrest

ClinicalTrials.gov ID: NCT00228293

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Official title

Assessment of Cardiopulmonary Resuscitation Quality During In-Hospital Cardiac Arrest

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Using an investigational monitor/defibrillator that passively records CPR quality parameters, including chest compression rate and depth and ventilation rate and volume, we are prospectively recording CPR quality during sequential in-hospital cardiac arrests at the University of Chicago Hospitals. Using an audio feedback system linked to this device, we are studying whether such audio feedback improves CPR quality when provided to rescuers trained in the use of the device.

Study identification

NCT ID: NCT00228293
Recruitment status: Terminated
Study type: Interventional
Phase: Phase 2, Phase 3
Lead sponsor: University of Chicago; Other
Enrollment: 200 participants

Conditions and interventions

Conditions

Cardiac Arrest

Interventions

investigational monitor/defibrillator with CPR feedback Device

Device

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Dec 2002 (Type not available)
Primary completion: Not listed
Completion: Sep 2005 (Type not available)
Last update posted: Sep 23, 2013

2002 – 2005

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
University of Chicago Hospitals	Chicago	Illinois	60637	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00228293, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Sep 23, 2013 · Synced Nov 15, 2026