Cardiogenic Shock AcuteHK CSINCT07323238
Hong Kong Cardiogenic Shock Initiative
An observational study of Cardiogenic Shock Acute and STEMI - ST Elevation Myocardial Infarction, run by Prince of Wales Hospital, Shatin, Hong Kong at 1 site in Hong Kong.
Trial summary
Acute myocardial infarction complicated by cardiogenic shock (AMI-CS) is a severe condition with high mortality. Early revascularization and Impella device (Abiomed) support improve outcomes. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cardiogenic Shock Acute, STEMI - ST Elevation Myocardial Infarction, Cardiogenic Shock
- How many people
- 320 participants
- Where
- 1 siteHong Kong
- Study dates
- 1 Dec 2026to 2 Oct 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: HKCSI will approximately include 320 cases over 5 years. For subjects in GCSI-eligible cohort (expect n=80), data will be shared with GCSI Study Team and performed together with their Global Database. Analysis of the whole HKCSI cohort will be conducted locally. Study sites will screen all acute myocardial infarction complicated by cardiogenic shock patients, NSTEMI and STEMI, for participation in this trial.
Who may be able to join
- Diagnosis of acute myocardial infarction (AMI) with the ECG and/or biomarker evidence of S-T elevation myocardial infarction (STEMI) or non -S-T elevation myocardial infarction (NSTEMI)
- Cardiogenic Shock is defined as presence of at least two of the following
- Hypotension (systolic blood pressure ≤ 100 mmHg, or inotropes/vasopressors to maintain systolic blood pressure ≥ 100 mmHg)
- Evidence of end organ perfusion: elevated serum lactate levels (venous or arterial), cool extremities, oliguria/anuria
- Hemodynamic criteria represented by cardiac index of <2.2 L/min/m² or a cardiac ≤ 0.6 watts
- Patient is supported with a transvalvular MCS as the initial device (criteria for GCSI-eligible Cohort)
- Patients undergo PCI within 12 hours of hospital presentation (criteria for GCSI-eligible Cohort)
- Subject or legally designated representative (LDR) has provided written informed consent. For patients not able to provide consent, data collection will be conducted in retrospective manner with study consent waived.
Who cannot join
- Unwitnessed out of hospital cardiac arrest or any cardiac arrest in which return of spontaneous circulation (ROSC) is not achieved within 20 minutes
- Patients demonstrate any signs of anoxic brain injury prior to the INDEX PCI (signs of anoxic injury include, posturing, seizures).
- IABP placed prior to MCS (criteria for GCSI-eligible Cohort)
- Septic, anaphylactic, hemorrhagic, and neurologic causes of shock
- Non-ischemic causes of shock/hypotension (pulmonary embolism, pneumothorax, myocarditis, tamponade, etc.)
- Active bleeding for which MCS in contraindicated
Show all 12Show fewer
- Recent major surgery for which MCS is contraindicated
- Mechanical complication of AMI (acute ventricular septal defect (VSD) or acute papillary muscle rupture)
- Known left ventricular thrombus for which MCS in contraindicated (criteria for GCSI-eligible Cohort)
- Mechanical aortic prosthetic valve (criteria for GCSI-eligible Cohort)
- Contraindication to intravenous systemic anticoagulation which precludes placement of MCS.
- Patients who fulfills all Eligibility Criteria would be recruited and considered GSCI-eligible. AMI-CS patients that did not use MCS, ie. Not fulfiliing both Inclusion Criteria 3, 4, would not be considered screen failure and would still be screened and recruited into HKCSI GCSI-ineligible cohort. Likewise, patients who meet any of Exclusion Criteria will not be GCSI-eligible. Specifically, patients who met exclusion criteria 3, 9, 10 only will be recruited into GCSI-ineligible cohort.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Acute myocardial infarction complicated by cardiogenic shock (AMI-CS) is a severe condition with high mortality. Early revascularization and Impella device (Abiomed) support improve outcomes. Observational studies like the National Cardiogenic Shock Initiative (NCSI), Inova-Shock registry, and J-PVAD (Japan registry for percutaneous ventricular assist device) registry emphasize the importance of structured care systems when using mechanical circulatory support (MCS).
Following the release of the Danger Shock trial, MCS use is expected to rise. Hospitals will need to monitor practices and work with payers to ensure coverage. Using regional real-world data can assist this process, making the collection and analysis of MCS outcomes essential.
Read more
The NCSI (NCT03677180) aimed to evaluate outcomes with a protocolized approach prioritizing rapid diagnosis, timely MCS delivery, and invasive hemodynamic monitoring via pulmonary artery (PA) catheters. The study involved 406 patients from 2016 to 2020, with an average age of 64 years. Most (67%) had shock, with 85% on vasoactive drugs. Witnessed outof-hospital cardiac arrest occurred in 17%, and in-hospital arrest in 30%. During MCS implantation, 9% were actively resuscitating. Patients mostly in SCAI stage C/D (73%) and stage E (27%) presented with low blood pressure, high lactate, and reduced cardiac power output. About 70% received MCS before PCI, with 90% using PA catheters. Most had STEMI, with median door-to-support and door-to-balloon times of about 78 and 81 minutes. Survival rates were high: 99% procedural, 79% to discharge, 77% at 30 days, and 62% at one year for stage C/D shock. Patients with stage E shock had lower survival. Early use of MCS improved hemodynamics and survival. Further research, like the CERAMICS (Can Escalation Reduce Acute Myocardial Infarction in Cardiogenic Shock) study, aims to refine escalation strategies. The Danger Shock trial highlighted the importance of minimizing complications such as bleeding, limb ischemia, haemolysis, and kidney injury.
Currently in Hong Kong, prevalence of CS among AMI patients is 5-10%, in-line with global statistics. Among which, 30-day and 1-year mortality of AMI-CS patients in Hong Kong was reported at 29% and 39.5% respectively. Although the use of MCS has been shown in the above overseas studies to improved survival rates of AMI-CS patients, the utilisation rate of MCS among AMI-CS patients in Hong Kong was reported at 36.5% in a previous single-centre study, limited by an array of factors including limited device availability, allocations of resources and patient selection strategy, lack of region-specific evidence and device affordability. Global Cardiogenic Shock Initiative (GCSI) is an ongoing international multicenter registry involving centers from USA, Germany, and Hong Kong, and focus on the outcomes of AMI-CS patients received Impella support. The GCSI is expanding to many other regions. In the Hong Kong Cardiogenic Shock Initiative (HK-CGSI) study we aim to include sites with experience in MCS, all of whom have the capability of MCS escalation and evaluate outcomes across these centers.
The goal is not only to capture the effects of previously established best practices but gain insights into regional best practices, and together with data from the global cardiogenic shock initiative (GCSI), to better establish the adoption of novel best practices and their effect on complication rates.
In parallel to GCSI-eligible cohort, i.e. Impella used as the first supporting device for patients with AMI-CS, given the significant portion of patients who could not receive MCS under current limitations in Hong Kong, in the HK-CSI, we will include also the GCSI-ineligible cohort, i.e. AMI-CSI without using Impella or not as the first MCS used, to understand the full picture of clinical outcomes of AMI-CS patients of Hong Kong.
The HK-CSI study is an observational registry solely and not a treatment study. This single-arm registry captures data generated during procedures which are considered standard of care. Participation in this registry will be performed with waiver of consent of the patient and will have no influence on the type and extent of treatment.
- Conditions
- Cardiogenic Shock Acute, STEMI - ST Elevation Myocardial Infarction, Cardiogenic Shock, Cardiogenic Shock Post Myocardial Infarction, Mechanical Circulatory Support
- Medical subject headings
- ST Elevation Myocardial Infarction, Shock, Cardiogenic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| GSCI-eligible | Cases that need mechanical cardiovascular support and meet all GSCI incluision and exclusion criterias | |
| GSCI-ineligible | All other cases with Cardiogenic shock but do not meet all GSCI incluision and exclusion criterias |
What is being measured
The primary outcome is the main question the study is designed to answer.
MCS escalation rate during index hospitalisation
MCS escalation rate of AMI-CS patient with use of MCS
Measured: Perioperative
1-year mortality
1-year mortality of AMI-CS patient with use of MCS
Measured: 1-year
1-year mortality
1-year mortality of AMI-CS patient without use of MCS
Measured: 1-year
30-day mortality
30-day mortality of AMI-CS patient without use of MCS
Measured: 30-day
30-day mortality
30-day mortality of AMI-CS patient with use of MCS
Measured: 30-day
Secondary outcomes (16)
180-day Mortality rate
180-day mortality rate of AMI-CS patient with use of MCS
Measured: 180-day
180-day Mortality rate
180-day mortality rate of AMI-CS patient without use of MCS
Measured: 180-day
30-day MCS escalation rate
MCS escalation rate of AMI-CS patient with use of MCS at 30-day
Measured: 30-day
180-day MCS escalation rate
MCS escalation rate of AMI-CS patient with use of MCS at 30-day
Measured: 180-day
360-day MCS escalation rate
MCS escalation rate of AMI-CS patient with use of MCS at 30-day
Measured: 360-day
Rate of In-Hospital Access Site Bleeding
Rate of In-Hospital Access Site Bleeding rated by BARC Bleeding Events during index hospitalization
Measured: Perioperative
Rate of acute kidney injury
Acute kidney injury (AKI) per KIDIGO (modified AKIN level >=2) during index hospitalization
Measured: Perioperative
Rate of Acute Limb Ischemia
Acute Limb Ischemia requiring fasciotomy and/or amputation during index hospitalization
Measured: Perioperative
Lactate level
Lactate Clearance during index hospitalization
Measured: Perioperative
Blood Transfusion rate
Rate of Blood Transfusion due to Consumption during index hospitalization
Measured: Perioperative
Blood Transfusion rate
Rate of Blood Transfusion due to Hemolysis during index hospitalization
Measured: Perioperative
MCS escalation rate
MCS escalation rate of AMI-CS patient with use of MCS During index hospitalisation
Measured: Perioperative
MCS escalation rate
MCS escalation rate of AMI-CS patient with use of MCS During index hospitalisation within 12 hours of hemodynamic findings
Measured: First 12 hours during index hospitalisation
Rate of MCS re-introduction after removal
Rate of MCS re-introduction after removal in AMI-CS patient with use of MCS
Measured: Perioperative until discharge
Access Site Complication rate
Rate of MCS Access Site Complications within 48 hours of MCS removal
Measured: within 48 hours of MCS removal
Access Site bleeding rate
Rate of MCS Access Site bleeding within 48 hours of MCS removal
Measured: within 48 hours of MCS removal
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Jan 2026
- Study start1 Dec 2026 (estimated)
- Primary completion1 Apr 2030 (estimated)
- Study completion2 Oct 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cardiogenic Shock AcuteStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Other
- Enrolment
- 320 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Prince of Wales Hospital, Shatin, Hong Kong
- Sponsor type
- University, hospital or other
- Collaborators
- Queen Elizabeth Hospital, Hong Kong, Tuen Mun Hospital, Hospital Authority, Hong Koong
- Responsible party
- Principal investigator, Dr So Chak Yu kent, Prince of Wales Hospital, Shatin, Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07323238
- Sponsor's protocol ID
- 2025.671
- Acronym
- HK CSI
- Status last verified
- Sep 2026
- First submitted
- 3 Dec 2025
- Last updated
- 16 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hong Kong Cardiogenic Shock Initiative
- ClinicalTrials.gov ID
- NCT07323238
- Acronym / sponsor ID
- HK CSI / 2025.671
- Conditions
- Cardiogenic Shock Acute, STEMI - ST Elevation Myocardial Infarction, Cardiogenic Shock, Cardiogenic Shock Post Myocardial Infarction, Mechanical Circulatory Support
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 320 participants (estimated)
- Lead sponsor
- Prince of Wales Hospital, Shatin, Hong KongUniversity, hospital or other
- Collaborators
- Queen Elizabeth Hospital, Hong Kong, Tuen Mun Hospital, Hospital Authority, Hong Koong
- Study start
- 1 Dec 2026 (estimated)
- Primary completion
- 1 Apr 2030 (estimated)
- Study completion
- 2 Oct 2030 (estimated)
- First posted
- 7 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Acute myocardial infarction complicated by cardiogenic shock (AMI-CS) is a severe condition with high mortality. Early revascularization and Impella device (Abiomed) support improve outcomes. Observational studies like the National Cardiogenic Shock Initiative (NCSI), Inova-Shock registry, and J-PVAD (Japan registry for percutaneous ventricular assist device) registry emphasize the importance of structured care systems when using mechanical circulatory support (MCS).
Following the release of the Danger Shock trial, MCS use is expected to rise. Hospitals will need to monitor practices and work with payers to ensure coverage. Using regional real-world data can assist this process, making the collection and analysis of MCS outcomes essential.
The NCSI (NCT03677180) aimed to evaluate outcomes with a protocolized approach prioritizing rapid diagnosis, timely MCS delivery, and invasive hemodynamic monitoring via pulmonary artery (PA) catheters. The study involved 406 patients from 2016 to 2020, with an average age of 64 years. Most (67%) had shock, with 85% on vasoactive drugs. Witnessed outof-hospital cardiac arrest occurred in 17%, and in-hospital arrest in 30%. During MCS implantation, 9% were actively resuscitating. Patients mostly in SCAI stage C/D (73%) and stage E (27%) presented with low blood pressure, high lactate, and reduced cardiac power output. About 70% received MCS before PCI, with 90% using PA catheters. Most had STEMI, with median door-to-support and door-to-balloon times of about 78 and 81 minutes. Survival rates were high: 99% procedural, 79% to discharge, 77% at 30 days, and 62% at one year for stage C/D shock. Patients with stage E shock had lower survival. Early use of MCS improved hemodynamics and survival. Further research, like the CERAMICS (Can Escalation Reduce Acute Myocardial Infarction in Cardiogenic Shock) study, aims to refine escalation strategies. The Danger Shock trial highlighted the importance of minimizing complications such as bleeding, limb ischemia, haemolysis, and kidney injury.
Currently in Hong Kong, prevalence of CS among AMI patients is 5-10%, in-line with global statistics. Among which, 30-day and 1-year mortality of AMI-CS patients in Hong Kong was reported at 29% and 39.5% respectively. Although the use of MCS has been shown in the above overseas studies to improved survival rates of AMI-CS patients, the utilisation rate of MCS among AMI-CS patients in Hong Kong was reported at 36.5% in a previous single-centre study, limited by an array of factors including limited device availability, allocations of resources and patient selection strategy, lack of region-specific evidence and device affordability. Global Cardiogenic Shock Initiative (GCSI) is an ongoing international multicenter registry involving centers from USA, Germany, and Hong Kong, and focus on the outcomes of AMI-CS patients received Impella support. The GCSI is expanding to many other regions. In the Hong Kong Cardiogenic Shock Initiative (HK-CGSI) study we aim to include sites with experience in MCS, all of whom have the capability of MCS escalation and evaluate outcomes across these centers.
The goal is not only to capture the effects of previously established best practices but gain insights into regional best practices, and together with data from the global cardiogenic shock initiative (GCSI), to better establish the adoption of novel best practices and their effect on complication rates.
In parallel to GCSI-eligible cohort, i.e. Impella used as the first supporting device for patients with AMI-CS, given the significant portion of patients who could not receive MCS under current limitations in Hong Kong, in the HK-CSI, we will include also the GCSI-ineligible cohort, i.e. AMI-CSI without using Impella or not as the first MCS used, to understand the full picture of clinical outcomes of AMI-CS patients of Hong Kong.
The HK-CSI study is an observational registry solely and not a treatment study. This single-arm registry captures data generated during procedures which are considered standard of care. Participation in this registry will be performed with waiver of consent of the patient and will have no influence on the type and extent of treatment.
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| GSCI-eligible | – | –Cases that need mechanical cardiovascular support and meet all GSCI incluision and exclusion criterias |
| GSCI-ineligible | – | –All other cases with Cardiogenic shock but do not meet all GSCI incluision and exclusion criterias |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- HKCSI will approximately include 320 cases over 5 years. For subjects in GCSI-eligible cohort (expect n=80), data will be shared with GCSI Study Team and performed together with their Global Database. Analysis of the whole HKCSI cohort will be conducted locally. Study sites will screen all acute myocardial infarction complicated by cardiogenic shock patients, NSTEMI and STEMI, for participation in this trial.
Key inclusion criteria (8 listed)
- Diagnosis of acute myocardial infarction (AMI) with the ECG and/or biomarker evidence of S-T elevation myocardial infarction (STEMI) or non -S-T elevation myocardial infarction (NSTEMI)
- Cardiogenic Shock is defined as presence of at least two of the following
- Patient is supported with a transvalvular MCS as the initial device (criteria for GCSI-eligible Cohort)
- Patients undergo PCI within 12 hours of hospital presentation (criteria for GCSI-eligible Cohort)
- Subject or legally designated representative (LDR) has provided written informed consent. For patients not able to provide consent, data collection will be conducted in retrospective manner with study consent waived.
Key exclusion criteria (12 listed)
- Unwitnessed out of hospital cardiac arrest or any cardiac arrest in which return of spontaneous circulation (ROSC) is not achieved within 20 minutes
- Patients demonstrate any signs of anoxic brain injury prior to the INDEX PCI (signs of anoxic injury include, posturing, seizures).
- IABP placed prior to MCS (criteria for GCSI-eligible Cohort)
- Septic, anaphylactic, hemorrhagic, and neurologic causes of shock
- Non-ischemic causes of shock/hypotension (pulmonary embolism, pneumothorax, myocarditis, tamponade, etc.)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
MCS escalation rate during index hospitalisation
Time frame: Perioperative
MCS escalation rate of AMI-CS patient with use of MCS
1-year mortality
Time frame: 1-year
1-year mortality of AMI-CS patient with use of MCS
1-year mortality
Time frame: 1-year
1-year mortality of AMI-CS patient without use of MCS
30-day mortality
Time frame: 30-day
30-day mortality of AMI-CS patient without use of MCS
30-day mortality
Time frame: 30-day
30-day mortality of AMI-CS patient with use of MCS
16 secondary outcomes
180-day Mortality rate
Time frame: 180-day
180-day Mortality rate
Time frame: 180-day
30-day MCS escalation rate
Time frame: 30-day
180-day MCS escalation rate
Time frame: 180-day
360-day MCS escalation rate
Time frame: 360-day
Rate of In-Hospital Access Site Bleeding
Time frame: Perioperative
Rate of acute kidney injury
Time frame: Perioperative
Rate of Acute Limb Ischemia
Time frame: Perioperative
Lactate level
Time frame: Perioperative
Blood Transfusion rate
Time frame: Perioperative
Blood Transfusion rate
Time frame: Perioperative
MCS escalation rate
Time frame: Perioperative
MCS escalation rate
Time frame: First 12 hours during index hospitalisation
Rate of MCS re-introduction after removal
Time frame: Perioperative until discharge
Access Site Complication rate
Time frame: within 48 hours of MCS removal
Access Site bleeding rate
Time frame: within 48 hours of MCS removal
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cardiogenic Shock Acute and STEMI - ST Elevation Myocardial Infarction, run by Prince of Wales Hospital, Shatin, Hong Kong at 1 site in Hong Kong.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 16 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Kent Chak Yu So (852-35051518, kentso987@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
MCS escalation rate during index hospitalisation (time frame: Perioperative). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Sep 2026.