Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:33 AM
Ignite Modification Date:
2025-12-25 @ 1:33 AM
NCT ID:
NCT06967194
Eligibility Criteria:
Inclusion Criteria:
* Diagnosis of ST-segment elevation myocardial infarction (STEMI) confirmed by ECG, clinical signs, and coronary catheterization.
* Post-catheterization patients classified as SCAI B upon admission to the unit, defined by the presence of tachycardia and/or hypotension without signs of hypoperfusion (i.e., normal lactate levels, normal capillary refill, preserved mental status, and adequate urine output \>0.5 mL/kg/hour).
* Age 18 years or older.
* Mentally competent to provide informed consent, understand the study procedures, and comply with medical recommendations.
Exclusion Criteria:
* Pregnancy.
* Inability to provide informed consent.
* Evidence of pulmonary edema.
* Bradycardia (heart rate \<60 beats per minute).
* PR interval \>240 milliseconds.
* Second- or third-degree atrioventricular (AV) block.
* Active asthma.
* Known hypersensitivity to metoprolol.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06967194
Study Brief:
Protocol Section:
NCT06967194