Hemodynamic monitoring improved the clinical outcomes of the patients with acute myocardial infarction complicated by cardiogenic shock

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200061375

Enrollment

Unknown

Registered

2022-06-22

Start date

2018-01-01

Completion date

Unknown

Last updated

2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute myocardial infarction complicated by cardiogenic shock

Interventions

control group:The pharmacological strategy was managed at the discretion of the attending physician according to clinical experience.

PiCCO group:The hemodynamic parameters were used to guide pharmacological treatment.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criteria were as follows: (1) age =18 years old; (2) signed the informed consent; and (3) patients diagnosed with AMICS.

Exclusion criteria

Exclusion criteria: The exclusion criteria included the following: (1) extensive peripheral vascular disease; (2) severe valve disease; (3) patient treated with extracorporeal membrane oxygenation (ECMO); (4) pregnant or lactating women; (5) enrolled in an additional clinical study; and (6) informed consent not obtained or noncompliance with follow-up.

Design outcomes

Primary

Measure	Time frame
major adverse cardiovascular and cerebrovascular events;	—

Secondary

Measure	Time frame
length of hospital stays;duration of mechanical ventilation, inotropes, diuretics, vasopressors, or vasodilators during hospitalization;changes of high-sensitive Troponin T (hs-TnT), N-terminal pro-brain natriuretic peptide (NT-proBNP), left ventricular ejection fraction (LVEF), serum creatinine (Scr) and alanine transaminase (ALT);	—

Countries

China

Contacts

Public ContactJieyun You

Shanghai East Hospital

youjieyun1118@hotmail.com+86 13917791748

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026