Health Condition 1: I211- ST elevation (STEMI) myocardial infarction of inferior wall Health Condition 2: I222- Subsequent non-ST elevation (NSTEMI) myocardial infarction Health Condition 3: I220- Subsequent ST elevation (STEMI) myocardial infarction of anterior wall
Conditions
Interventions
Intervention1: NIL: NIL
Sponsors
STEMI India group
Eligibility
Inclusion criteria
Inclusion criteria: All patients presenting to the emergency room with chest pain and a provisional diagnosis of ACS above the age of 18 years. Signed informed consent form prior to trial participation
Exclusion criteria
Exclusion criteria: Patients with provisional diagnosis other than ACS Patient not willing to give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sensitivity, specificity, positive predictive value and negative predictive value of changes in high frequency ECG (need to define it) as compared to hs-cTnTimepoint: Baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| • In STEMI patients, 90minute Post thrombolysis HF-ECG as compared to standard ECG to assess success of thrombolysis. • Return to normal of HF-ECG (90 minute and 12–24-hour ECG) to normal as compared to standard ECG and abnormal HF-ECG (recorded prior to reperfusion) following reperfusion of culprit vessel for failed reperfusion or after primary PCI. • Return to normal HF-ECG as compared to standard ECG and abnormal HF-ECG (recorded prior to reperfusion) after reperfusion of culprit vessel in NSTEMI/UA Timepoint: 12-24 hours of Post PCI | — |
Countries
India
Contacts
Public ContactDr Ajit MullasariS
The Madras Medical Mission
Outcome results
None listed