Skip to main content
TTrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor.
RECRUITINGOBSERVATIONAL

Stunning in Takotsubo Versus Acute Myocardial Infarction

STAMI- Stunning in Takotsubo Versus Acute Myocardial Infarction

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The Stunning in Takotsubo versus Acute Myocardial Infarction (STAMI) Study Background: Acute myocardial stunning, herein defined as the reversible loss of myocardial function, occurs in both takotsubo syndrome (TS) and ST-elevation myocardial infarction (STEMI), and can be life-threatening in both conditions. However, despite typically having considerably more pronounced myocardial stunning, TS patients have better prognosis than patients with STEMI. Despite the different relationship between extent of myocardial stunning and prognosis in TS vs STEMI, no 'head-to-head' comparison of the myocardial stunning phenotypes in TS vs STEMI has been done. Methods: The Stunning In Takotsubo and Acute Myocardial Infarction (STAMI) study is a single-center, prospective clinical study that will enroll 100 patients with STEMI and 25 patients with TS. Echocardiography, laboratory testing (including troponin and NTpro-BNP), and ECG will be done immediately after angiography and at days 1, 2, 3, 7, 14 and 30. The primary endpoint is the proportion of myocardial stunning that has resolved after 72 hours, as determined by echocardiography. Total myocardial stunning is defined as the extent of akinesia observed at day 0 that resolves by day 30.

Who May Be Eligible (Plain English)

Who May Qualify: - STEMI or TS with planned coronary angiography within 12 hours from the onset of symptoms - Written consent Who Should NOT Join This Trial: - Cardiogenic shock, defined as Killip class IV - Expected inability to comply with the protocol Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * STEMI or TS with planned coronary angiography within 12 hours from the onset of symptoms * Written consent Exclusion Criteria: * Cardiogenic shock, defined as Killip class IV * Expected inability to comply with the protocol

Treatments Being Tested

DIAGNOSTIC_TEST

Echocardigraphy (ECHO)

Standar 12 lead electrocardiogram

DIAGNOSTIC_TEST

Bloodtest

cardiac biomarkers

Locations (1)

Department of Cardiology; Sahlgrenska University Hospital
Gothenburg, Sweden