NCT04110912

Brief Summary

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.

Trial Health

50
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
178mo left

Started Jan 2015

Longer than P75 for all trials

Geographic Reach
1 country

3 active sites

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress44%
Jan 2015Dec 2040

Study Start

First participant enrolled

January 1, 2015

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

March 2, 2017

Completed
2.6 years until next milestone

First Posted

Study publicly available on registry

October 1, 2019

Completed
21.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2040

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2040

Last Updated

October 1, 2019

Status Verified

September 1, 2019

Enrollment Period

25.9 years

First QC Date

March 2, 2017

Last Update Submit

September 30, 2019

Conditions

Keywords

Cardiac arrest, Trauma, Acute stroke, and Sepsis

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (4)

  • Effectiveness and Translation

    1 year (annual)

  • Evaluation

    1 year (annual)

  • International Collaboration in both Efficacy and Effectiveness

    1 year (annual)

  • Examine epidemiologic and outcomes

    1 year (annual)

Study Arms (4)

Cardiac arrest

Ischaemic heart disease is the leading cause of death worldwide. However, this is a registry and no interventions are taking place

Other: This is a registry and no interventions are taking place.

Trauma

Worldwide, trauma is the number one cause of death and disability in people younger than 40 and confirmed for Canada as well for those under the age of 45. However, this is a registry and no interventions are taking place

Other: This is a registry and no interventions are taking place.

Sepsis

Sepsis is a clinical syndrome that results from dysregulation of the inflammatory response to severe infection. However, this is a registry and no interventions are taking place

Other: This is a registry and no interventions are taking place.

Stroke

Stroke is the second leading cause of death worldwide, and the leading cause of chronic disability. However, this is a registry and no interventions are taking place

Other: This is a registry and no interventions are taking place.

Interventions

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All persons within the catchment area of any EMS agency participating, including infants, children and adult patients requiring activation of the emergency 9-1-1 system that meet the defined criteria for cardiac arrest, traumatic injury, stroke or sepsis.

You may qualify if:

  • Cardiac Arrest Eligibility
  • 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
  • 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
  • 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
  • +7 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Hamilton Health Sciences

Hamilton, Ontario, L8V 1C3, Canada

Location

Sunnybrook Health Sciences Center

Toronto, Ontario, M4N 3M5, Canada

Location

St Michael's Hospital

Toronto, Ontario, M5V 1W8, Canada

Location

Related Publications (3)

  • 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 2011 Jan 26.

  • 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. doi: 10.1111/acem.13032. Epub 2016 Sep 27.

  • 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.

MeSH Terms

Conditions

Heart ArrestSepsisWounds and InjuriesStroke

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesInfectionsSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and SymptomsCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular Diseases
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 2, 2017

First Posted

October 1, 2019

Study Start

January 1, 2015

Primary Completion (Estimated)

December 1, 2040

Study Completion (Estimated)

December 1, 2040

Last Updated

October 1, 2019

Record last verified: 2019-09

Data Sharing

IPD Sharing
Will share

Locations