Monitoring of Intubation and Ventilation During Resuscitation
1 other identifier
interventional
15
1 country
1
Brief Summary
Airway control and ventilation is vital during cardiopulmonary resuscitation (CPR) in cardiac arrest. Endotracheal intubation is the gold standard for airway control, but several studies have shown high rates of unrecognized placements of the tube in the esophagus instead of in the airway out-of-hospital. This is lethal. There are no failproof technique for recognising such mistakes clinically in the cardiac arrest situation. Changes on the air volume in the lungs with ventilation changes the impedance (resistance to alternating current) through the thorax. This impedance is already measured routinely by the defibrillators used during CPR. We propose that we can measure ventilation volumes and also discover failed intubations by monitoring this impedance during CPR with the possibility of giving feedback on both to the rescuers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_2
Started Sep 2004
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2004
CompletedFirst Submitted
Initial submission to the registry
September 12, 2005
CompletedFirst Posted
Study publicly available on registry
September 20, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2007
CompletedAugust 27, 2007
August 1, 2007
September 12, 2005
August 24, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
sensitivity/specificity for lung ventilation detection
correlation ventilation volume - impedance change
Interventions
Eligibility Criteria
You may qualify if:
- Cardiac arrest
You may not qualify if:
- \<18 years old trauma pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Oslolead
- Laerdal Medicalcollaborator
- Ullevaal University Hospitalcollaborator
- Health Region East, Norwaycollaborator
- Norwegian Air Ambulance Foundationcollaborator
- University of Stavangercollaborator
Study Sites (1)
Ulleval University Hospital
Oslo, N-0407, Norway
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Elizabeth Dorph
Ulleval University Hospital, University of Oslo
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 12, 2005
First Posted
September 20, 2005
Study Start
September 1, 2004
Study Completion
April 1, 2007
Last Updated
August 27, 2007
Record last verified: 2007-08