Could Hands-Only CPR be just as good as standard CPR?
NCT ID NCT03981107
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two types of CPR for people who have a cardiac arrest outside a hospital: hands-only CPR (chest compressions without rescue breaths) versus standard CPR (compressions plus rescue breaths). The trial will include over 3,000 adults whose cardiac arrest is witnessed and who have a bystander with prior CPR training. The goal is to see if hands-only CPR is at least as effective as standard CPR at helping people survive for 30 days.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Chest compression only CPR (hands-only CPR)
- What this could lead to
- If hands-only CPR works as well as standard CPR, it could simplify training and encourage more bystanders to act, potentially saving more lives from cardiac arrest.
- What could go wrong
- This is a large trial, but it only includes trained bystanders and witnessed arrests. Results may not apply to all situations, and hands-only CPR might be less effective for certain causes of cardiac arrest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 3,260 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2017
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Unconsciousness with no, abnormal or agonal breathing (suspected OHCA) * The suspected OHCA is witnessed (seen or heard) * Any Bystander at the scene has previous training in CPR Exclusion Criteria: * Age below 18 years * Collapse is not witnessed * Bystander has no prior CPR training * Obvious asphyxia (i.e. hanging, foreign body, suffocation, strangulation) * Obvious drug overdose / intoxication * Pregnancy * Trauma (penetrating, blunt, burn injury) Post randomisation exclusion Criteria from data analysis: * Not EMS-verified cardiac arrest * Previous do not resuscitate (DNR) decision
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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AREU, Agenzia Regionale Emergenza Urgenza
RECRUITINGBergamo, Italy
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SOS Alarm AB
RECRUITINGStockholm, Sweden
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