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Clinical Trials/NCT07266675
NCT07266675RecruitingNot Applicable

Post-Acute Phase of Cardiogenic Shock (PACS) Registry

Mackay Memorial Hospital1 site in 1 country350 target enrollmentStarted: July 19, 2024Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
350
Locations
1
Primary Endpoint
mortality
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Epidemiology studies showed that the burden of cardiogenic shock (CS) persistently high, with increasing annual medical expenses and steady prevalence. In-hospital and one-year mortality reduce annually. Hence, there are increasing number of patients who survive to hospital discharge but they will face further challenges in the subacute stage after hospital discharge. However, there are still insufficient studies focusing on this issue. Establishment of a healthcare neatwork to help hospital survivors of CS return society safely is critical.

Detailed Description

Multicener, prospective cohort study

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Hospital survivors of cardiogenic shock

Exclusion Criteria

  • •Age < 18 years。
  • •Patient or family refuse follow-up.
  • •Patient died within hospital stay.

Outcomes

Primary Outcomes

mortality

Time Frame: 1 year

any death

rehospitalization

Time Frame: 1 year

any rehospitalization

Secondary Outcomes

  • mortality(180-day)
  • rehospitalization(180-day)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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