- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02184468
Survival Study After Out-of-hospital Cardiac Arrest (SAMS)
Dual Dispatch of EMS, Fire Fighters and/or Police in Out-of-hospital Cardiac Arrest Implemented in Nine Counties in Sweden - Can More Lives be Saved by Using This Method?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hypothesis If simultaneous dispatch of ambulance (EMS), firefighters and/or police is being initiated when an OHCA occurs, then the two latter units will be first at scene, before the ambulance crew, in ≥30% of the cases. We anticipate therefore that overall 30-days survival will increase on a national level from 9% to 12%.
Method During the period 110901 to 141231 all OHCA cases will be analyzed were the emergency medical communication centre (EMCC) has dispatched ambulance, firefighters and/or the police. Participating in the Saving More Lives in Sweden (SAMS) project are the following counties: Stockholm, Sodermanland, Jonkoping, Vastra Gotaland (VG Region), Halland, Dalarna, Jamtland, Kalmar and Uppsala. Data is collected by the units being dispatched and thereafter sent on line to a database managed by Registercentrum in Gothenburg (http://www.registercentrum.se/), administrators of the Swedish Cardiac Arrest Register.
Parameters obtained are:
- Time for dispatch of fire fighters and/or police (recorded digitally).
- Time for arrival to the patient.
- Verification if cardiac arrest or not.
- CPR performed by fire fighters or police before arrival of EMS.
- Automated External Defibrillator (AED) connected to the patient.
- If yes, was the first recorded rhythm shockable, i.e. ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT).
- Time to defibrillation.
Survival data during from the Swedish Cardiac Arrest Register (SCAR) will be obtained during the same time period from nine comparable Swedish regions not participating in the SAMS study.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Leif Svensson
- Phone Number: +4686161000
- Email: leif.svensson@ki.se
Study Contact Backup
- Name: Johan Herlitz
- Phone Number: +46334354000
- Email: johan.herlitz@gu.se
Study Locations
-
-
-
Stockholm, Sweden, SE-11883
- Recruiting
- Center for Resuscitation Science, Sodersjukhuset
-
Contact:
- Leif Svensson, MD, PhD
- Phone Number: +4686161000
- Email: leif.svensson@ki.se
-
Contact:
- Johan Herlitz, MD, PhD
- Phone Number: +46334354000
- Email: johan.herlitz@gu.se
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All cases where the dispatcher suspects cardiac arrest, i.e. unconscious person with abnormal or no breathing
Exclusion Criteria:
- Children < 8 y
- Obviously deceased persons according to regulations in EMS protocols
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Dual dispatch
Simultaneously dispatching of EMS, firefighters and/or police in OHCA
|
In case of OHCA, firefighters and/or police trained in CPR and equipped with AEDs will be dispatched in parallel with EMS in nine counties in Sweden.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Survival
Time Frame: 30-days after out-of-hospital cardiac arrest (OHCA)
|
30-days after out-of-hospital cardiac arrest (OHCA)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time for dispatching of fire fighters and/or police
Time Frame: Up to 1 y after ending recruitement
|
Data are obtained digitally from the dispatch center.
|
Up to 1 y after ending recruitement
|
Time for arrival to the patient
Time Frame: Up to 1 y after ending recruitement
|
Data are collected both digitally from the dispatch center and from protocols sent in on line by first responders.
|
Up to 1 y after ending recruitement
|
Time for attaching the defibrillator to the patient
Time Frame: Up to 1 y after ending recruitement
|
Data are collected from protocols sent in on line by first responders.
|
Up to 1 y after ending recruitement
|
Time to first defibrillation
Time Frame: Up to 1 y after ending recruitement
|
Data collected from the protocol sent in on line by first responders.
|
Up to 1 y after ending recruitement
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Leif Svensson, MD, PhD, Center for Resuscitation Science, Karolinska Institutet, Stockholm, Sweden
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SAMS 242-11
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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