Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
80 participants
OBSERVATIONAL
2017-02-24
2019-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of the Quality of Cardio-Pulmonary Resuscitation (CPR) in Cardiac Arrest Patients
NCT00951704
Synergy of Elevation of the Head and Thorax and REBOA During Out-of-Hospital Cardiac Arrest
NCT06537492
Resuscitation Enhancement to Avoid Rearrest Through Evidence-based Strategies in Prehospital Post-resuscitation Care
NCT07239908
Blood Pressure and Cerebral Blood Flow After Cardiac Arrest
NCT05434910
Hyperoxia Before and After Cardiac Arrest and Myocardial Damage
NCT03571074
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Standard cardiopulmonary resuscitation
Standard Advanced Life Support based on guidelines 2015, including mechanical chest compression device
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* resuscitation will be continued at least 5 minutes (if return of spontaneous circulation not achieved earlier) after arrival of physician team
Exclusion Criteria
* return of spontaneous circulation achieved before physician-led critical team arrives
* external cause for cardiac arrest (e.g. trauma, suffocation)
* workload too high or environment too dangerous to perform study procedures
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Helsinki University Central Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jouni Nurmi, MD
Consultant in Anaesthesia and Intensive Care Medicine
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jouni Nurmi, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Helsinki University Central Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
FinnHEMS 10, Emergency Medicine and Services, Helsinki University Hospital
Vantaa, , Finland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
54/13/03/02/16
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.