Stroke Clinical Trial
Official title:
Improving Outcomes After Time Sensitive Prehospital Interventions: Rescu Epistry
NCT number | NCT04110912 |
Other study ID # | Rescu Epistry |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | January 2015 |
Est. completion date | December 2040 |
Verified date | September 2019 |
Source | St. Michael's Hospital, Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Rescu Epistry includes data points pertaining to prehospital and in-hospital clinical treatments and responses to therapy, survival to discharge and functional outcome data for all cases.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2040 |
Est. primary completion date | December 2040 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: Cardiac Arrest Eligibility 1. Individuals of all ages who experience cardiac arrest outside the hospital, with evaluation by organized EMS personnel and: - Attempts at external defibrillation (by lay responders or emergency personnel), or chest compressions by organized EMS personnel (treated cohort) - Were pulseless but did not receive attempts to defibrillate or CPR by EMS personnel (untreated cohort - obviously dead by legislative definition) Traumatic Injury Eligibility 2. Individuals of all ages who experience a traumatic injury outside the hospital, with evaluation by organized EMS personnel and: - Systolic blood pressure = 90 mmHg or - Glasgow Coma Scale score =12 or - Respiratory rate <10 or >29 breaths per minute or - Field intubation/advanced airway procedure Stroke Eligibility 3. individuals of all ages who experience stroke outside the hospital, with evaluation by organized EMS personnel and new onset of signs and symptoms suggestive of an acute stroke - Unilateral arm/leg weakness or drift or - Slurred speech or inappropriate words or mute or - Unilateral facial droop Sepsis Eligibility 1. Potentially Septic: Individuals of all ages who present with - Presence of Fever: Temperature >38°C (tympanic membrane) - Paramedic suspects possible infection: i.e. suspected pneumonia, urinary tract infection, abdominal pain or distension, meningitis, cellulitis, septic arthritis, infected wound (minimal data set ) 2. Severe Sepsis: Individuals of all ages who also present with: - Presence of Fever: Temperature >38°C (tympanic membrane) - Paramedic suspects possible infection: e.g. suspected pneumonia, urinary tract infection, abdominal pain or distension, meningitis, cellulitis, septic arthritis, infected wound; Presence of any one of: (1) respiratory rate > 22/min or intubated for respiratory support; (2) acute confusion or reduced level of consciousness; (3) presence of hypotension: SBP<=100mmHg (comprehensive data set) Exclusion Criteria: None, |
Country | Name | City | State |
---|---|---|---|
Canada | Hamilton Health Sciences | Hamilton | Ontario |
Canada | St Michael's Hospital | Toronto | Ontario |
Canada | Sunnybrook Health Sciences Center | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto | Canadian Institutes of Health Research (CIHR), Heart and Stroke Foundation of Canada |
Canada,
Lin S, Morrison LJ, Brooks SC. Development of a data dictionary for the Strategies for Post Arrest Resuscitation Care (SPARC) network for post cardiac arrest research. Resuscitation. 2011 Apr;82(4):419-22. doi: 10.1016/j.resuscitation.2010.12.006. Epub 20 — View Citation
Lin S, Turgulov A, Taher A, Buick JE, Byers A, Drennan IR, Hu S, J Morrison L. Automated Data Abstraction of Cardiopulmonary Resuscitation Process Measures for Complete Episodes of Cardiac Arrest Resuscitation. Acad Emerg Med. 2016 Oct;23(10):1178-1181. d — View Citation
Sun CL, Demirtas D, Brooks SC, Morrison LJ, Chan TC. Overcoming Spatial and Temporal Barriers to Public Access Defibrillators Via Optimization. J Am Coll Cardiol. 2016 Aug 23;68(8):836-45. doi: 10.1016/j.jacc.2016.03.609. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Data Registry | To collect comprehensive, standardized, multicentre prehospital data to guide future EMS and Fire as well as in-hospital care (e.g. Emergency Department (ED), Trauma Room, Critical Care Units (CrCU), ward care and rehabilitation) for cardiac arrest, trauma, stroke, and sepsis patients. | 1 year (annual) | |
Secondary | Effectiveness and Translation | To evaluate the relationships between outcome and regionalized patient care systems, identify best practices, and compliance with guidelines and scientific statements or current evidence. (Effectiveness and Translation) | 1 year (annual) | |
Secondary | Evaluation | To use Rescu Epistry as the data collection interface to enable the evaluation of innovative strategies, including drugs, techniques and technology, and system changes to treat acutely ill patients with cardiac arrest, trauma, stroke, and sepsis in the prehospital setting through for example cohort studies, controlled clinical trials, and knowledge translation implementation trials. (Efficacy) | 1 year (annual) | |
Secondary | International Collaboration in both Efficacy and Effectiveness | To expand Rescu Epistry data collection to include other regions of care in Canada to provide provincial and national data sets and opportunities to collaborate internationally when increased sample sizes and cross border comparisons are required to advance the science quickly. | 1 year (annual) | |
Secondary | Examine epidemiologic and outcomes | To examine epidemiologic and outcomes aspects of acutely ill patients by linking Rescu Epistry to the existing health administrative data in Ontario contained at the Institute for Clinical Evaluative Sciences. | 1 year (annual) |
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