Intravenous Isosorbide Dinitrate Versus Sublingual Isosorbide Dinitrate for the Relief of Acute Anginal Episodes in Acute Coronary Syndrome (ACS) Patients
Unstable Angina, Myocardial Infarction
About this trial
This is an interventional treatment trial for Unstable Angina
Eligibility Criteria
Inclusion Criteria: Age > 18 years or older. Admission to the ICCU with ACS (non-ST elevation acute coronary syndrome or 24 hours after ST elevation myocardial infarction) . Presence of ischemic symptoms (≥5 minutes) during hospitalization. Pain assessment of 3 out of 10 on Visual Analog Scale (VAS) 1 or dynamic ECG findings (ST segment deviation ≥0.05 mV or T wave inversion ≥ 0.3 mV) Willing and able to provide written informed consent according to the regulations of the Ministry of Health and the Helsinki committee instructions. - Exclusion Criteria: Patient who meet any of the following criteria are excluded from the study: Persistent ST-segment elevation ≥ 1 mV in 2 or more contiguous leads or new LBBB. Acute pulmonary edema Sepsis Sustained systolic blood pressure < 90 mm Hg or evidence of cardiogenic shock Pregnant women Use at randomization of agents known to enhance the efficacy of nitrates. Clinically significant aortic stenosis Cr > 2 mg/dL Participation in another trial of an investigational drug or device on randomization. Allergy or sensitivity to nitatrate compounds Acute episode of cerebrovascular attack Inability to comply with the protocol and follow-up -
Sites / Locations
- Intensive Cardiac Care Unit