Clinical Outcome and Cost-effectiveness of Reduced Noradrenaline by Using a Lower Blood Pressure Target in Patients With Cardiogenic Shock From Acute Myocardial Infarction

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

Rationale: Pump failure due to acute myocardial infarction (AMI) can lead to cardiogenic shock (CS): a state of low blood flow to end-organs with subsequent multi-organ failure that is associated with high mortality rated. The first line pharmacologic treatment strategy in CS is noradrenaline. This vasopressor drug is used to maintain adequate blood pressures. The assumption is that a mean arterial blood pressure (MAP) ≥ 65 mmHg will improve flow and thereby tissue perfusion of myocardium and other tissues (e.g. renal). However, there is no evidence that an increase in MAP, if achieved by noradrenaline, leads to greater end-organ blood flow and better outcomes.

Objective: With this study the investigators aim to investigate the (cost-)effectiveness of reduced noradrenaline in patients with CS by using a lower MAP target of ≥ 55 mmHg, compared to ≥ 65 mmHg. The investigators hypothesize that reduced use of noradrenaline will improve overall survival and decrease renal failure requiring renal replacement therapy.

Study design: Open label, randomized controlled multicenter trial

Study population: Adults patients with CS due to AMI

Intervention: Treatment strategy of reduced noradrenaline, by using a lower MAP target ( ≥ 55 mmHg).

Main study endpoint: composite of all-cause mortality and severe renal failure leading to renal replacement therapy within 30-days after randomization.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Acute myocardial infarction, STEMI or NSTEMI

Early revascularization by PCI

Altered mental status

Cold, clammy skin and extremities

Disqualifiers

Resuscitation > 30 minutes

Mechanical cause of cardiogenic shock (e.g. papillary muscle rupture, ventricular septal rupture)

Onset of shock > 12 hours

Imminent need for mechanical circulatory support (i.e. ECPR)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Reduced noradrenaline use

    Drug

    Reduced noradrenaline by using a lower MAP target

Treatment groups

776 Participants
are divided into 2 treatment groups
Group A: Reduced noradrenaline (MAP ≥ 55 mmHg)Experimental treatment 1 intervention
Group B: Usual care (MAP ≥ 65 mmHg)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Mortality and renal failure

Composite of all-cause mortality and severe renal failure leading to renal replacement therapy

Time frame
30-days

Secondary outcomes

1

Blood pressure (systolic and diastolic)

Blood pressure measured hourly during the first 24 hours of ICU/CCU admission

Time frame
The first 24 hours
2

Heart rate

Heart rate, measured hourly during the first 24 hours of ICU/CCU admission

Time frame
The first 24 hours
3

Enzymatic infarct size, measured by hs-Troponin T

Size of myocardial infarction, measured by hs-Troponin T

Time frame
0, 6, 12, 24, 36 and 72 hours
4

Enzymatic infarct size, measured by CK-MB

Size of myocardial infarction, measured by CK-MB

Time frame
0, 6, 12, 24, 36 and 72 hours

Other outcomes

Sponsors and contacts

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