Post-Acute Phase of Cardiogenic Shock

November 24, 2025 updated by: Mackay Memorial Hospital

Post-Acute Phase of Cardiogenic Shock (PACS) Registry

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.

Study Overview

Status

Recruiting

Conditions

Detailed Description

Multicener, prospective cohort study

Study Type

Observational

Enrollment (Estimated)

350

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Taipei, Taiwan, 104217
        • Recruiting
        • MacKay Memorial Hospital
        • Contact:
          • Shih-Chieh Chien, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Hospital survivors of cardiogenic shock

Description

Inclusion Criteria:

Hospital survivors of cardiogenic shock

Exclusion Criteria:

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
mortality
Time Frame: 1 year
any death
1 year
rehospitalization
Time Frame: 1 year
any rehospitalization
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
mortality
Time Frame: 90-day
any death
90-day
rehospitalization
Time Frame: 90-day
any rehospitalization
90-day
mortality
Time Frame: 180-day
any death
180-day
rehospitalization
Time Frame: 180-day
any rehospitalization
180-day

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality
Time Frame: 1 year
KCCQ
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Cardiovascular department, MacKay Memorial Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 19, 2024

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

June 30, 2028

Study Registration Dates

First Submitted

November 24, 2025

First Submitted That Met QC Criteria

November 24, 2025

First Posted (Actual)

December 5, 2025

Study Record Updates

Last Update Posted (Actual)

December 5, 2025

Last Update Submitted That Met QC Criteria

November 24, 2025

Last Verified

October 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

need further discussion with other PI

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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