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CompletedNCT05414643Team-ShockUpdated Jun 10, 2022

Management of Acute Cardiogenic Shock at the New Brunswick Heart Centre

An observational study in Cardiogenic Shock, sponsored by New Brunswick Heart Centre. Completed at 1 site in Canada. Per ClinicalTrials.gov, last updated 2022-06-10.

Sponsored by New Brunswick Heart Centre · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,416
Sex
All
01

Study summary

In Atlantic Canada, acute myocardial infarction occurs at a rate of 2.9 % of the population and is the most common cause of cardiogenic shock (CS). In many studies, acute myocardial infarction accounts for up to 80% of the patients with CS. While there are different methods of treating patients with CS, the rate of mortality has not significantly improved over the years and remains as high as 50%. Recent studies have shown that a multi-modal, team-based approach can help improve patient outcomes; however, such a standardized approach is yet to be implemented in the New Brunswick Heart Centre (NBHC).

The study aims to understand the difference in outcomes between two groups of patients treated for CS: SHOCK TEAM versus non-SHOCK TEAM. This is a retrospective study of 168 patients using the data from NBHC registry and patient charts. The study duration is 1 year. The primary outcome is hospital survival. Secondary outcomes include time from diagnosis to invasive monitoring and intervention. All data will be analyzed statistically between the two groups. The end goal of the study is to establish standard guidelines to treat CS patients and improve patient survival.

02

Conditions studied

  • Cardiogenic Shock

Keywords

  • mortality
  • outcomes
  • AMI
  • shock team
  • SCAI stage
  • intervention
  • IABP
  • ECMO
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In context

Shock, Cardiogenic

277 studies on the registry are indexed under Shock, Cardiogenic; 127 are open to participants now.

This study's enrollment of 1,416 is above the median of 200 across 142 observational studies indexed under Shock, Cardiogenic.

Browse Shock, Cardiogenic studies →

Lead sponsor

New Brunswick Heart Centre is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients who were admitted to the CCU at the NBHC, Saint John Regional Hospital between November 1st 2019 to November 30th 2020 were included in the study.

Inclusion criteria

  1. Any patient admitted to the CCU with a diagnosis of CS (SCAI groups C, D or E) at any point during their CCU care.

Exclusion criteria

Exclusion Criteria:

  1. CS patients having SCAI groups A, B (this group was used only for preliminary analysis, hence this is the exclusion criteria for all final analyses).
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,416 participants (actual)
Patient registry
No

Groups and cohorts

  • At- risk group (SCAI stages A, B)

    Patients who had a SCAI stage A or B at any point during their stay at the New Brunswick Heart Centre, Saint John Regional Hospital. This group was compared with the cardiogenic shock group only for preliminary analysis.

    Other: Standard care

  • Cardiogenic shock group (SCAI stages C-E)

    Patients who had a SCAI (Society for Cardiovascular Angiography and Interventions) stage C-E at any point during their stay at the New Brunswick Heart Centre, Saint John Regional Hospital. This group was used for all subsequent analyses.

    Other: Standard care

Interventions

  • OtherStandard care

    No interventions were used, as this is an observational study.

06

What researchers measure

Primary outcomes

  1. Percentage mortality

    Any in-hospital mortality (within Saint John Regional Hospital, another hospital after transfer)

    Time frame: From the date of hospital admission at Saint John Regional Hospital to the date of discharge, assessed upto 6 months

  2. Length of stay (LOS))

    LOS was considered only for patients who were discharged directly home from Saint John Regional Hospital

    Time frame: From the date of hospital admission at Saint John Regional Hospital to the date of discharge, assessed upto 6 months

  3. Discharge disposition

    Discharge of patients home, transfer to another hospital or to another institution (special care home, extra-mural home)

    Time frame: From the date of hospital admission at Saint John Regional Hospital to the date of discharge, assessed upto 6 months

  4. Percentage of missed opportunities

    Missed opportunities was defined as patients who suffered significant delays or those who did not receive any intervention

    Time frame: From the date of hospital admission at Saint John Regional Hospital to the date of discharge, assessed upto 6 months

Secondary outcomes

  1. Time from diagnosis of shock to in-hospital processes

    Time gaps between the first diagnosis of a cardiogenic shock to in-hospital processes like invasive monitoring, cardiac catheterization or interventions (surgery, PCI, TAVI, IABP or ECMO).

    Time frame: From the date of hospital admission at Saint John Regional Hospital to the date of discharge, assessed upto 6 months

07

Study locations

1 site
  • New Brunswick Heart Centre
    Saint John, New Brunswick E2L 4L2, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05414643
Lead sponsor
New Brunswick Heart Centre
Responsible party
Dr. Jean-François Légaré (Head of Cardiac Surgery, New Brunswick Heart Centre) — Principal investigator
First posted
Jun 10, 2022
Start date
Jan 14, 2021
Primary completion
Oct 13, 2021
Completion
Oct 13, 2021
Last update
Jun 10, 2022

Study contacts

Jean-François Légaré, M.D., Ph.D.
principal investigator · New Brunswick Heart Centre

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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