Phase 2
N=1,586
Automated Real-time Feedback on CPR Study
Heart Arrest
Bottom Line
View on ClinicalTrials.gov: NCT00539539 ↗Enrolled (actual)
1,586
Serious AEs
0.0%
Results posted
Jun 2012
Primary outcome: Primary: Rate of ROSC During the Prehospital Resuscitation — 361; 345 Participants — p=0.96
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Laerdal Q-CPR /technology (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Washington
- Primary completion
- Jun 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Rate of ROSC During the Prehospital Resuscitation |
361; 345 | 0.96 |
| SECONDARY Pulses Present at ED Arrival. |
260; 243 | 0.71 |
| SECONDARY Survival to Hospital Discharge |
92; 96 | 0.21 |
| SECONDARY CPR Fraction |
66; 64 | 0.016 sig |
| SECONDARY Compression Depth |
39.6; 37.8 | 0.005 sig |
| SECONDARY Compression Rate |
103.1; 108.0 | <0.001 sig |
| SECONDARY Percentage of Compressions With an Incomplete Release |
10.4; 14.6 | <0.001 sig |
| SECONDARY Ventilation Rate |
5.8; 5.6 | 0.73 |
Summary
The purpose of this study is to evaluate whether or not real-time feedback on CPR process variables will increase rates of restoration of spontaneous circulation during prehospital resuscitation and upon arrival at the receiving emergency room as well as increase rates of survival to hospital discharge.
Eligibility Criteria
Inclusion Criteria
- all individuals who experience cardiac arrest outside the hospital,
- are evaluated by organized EMS personnel and: a) receive attempts at external defibrillation (by lay responders or emergency personnel) or receive chest compressions by organized EMS personnel.
Exclusion Criteria
- Use of a mechanical CPR device
Data sourced from ClinicalTrials.gov (NCT00539539). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.