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Study identifier: NCT06967194 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Early Beta Blocker Administration in STEMI Patients With SCAI B Status

Condition: ST Segment Elevation Myocardial Infarction (STEMI) · Cardiogenic Shock Post Myocardial Infarction  ·  Sponsor: Tel-Aviv Sourasky Medical Center

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is looking at how a medication called beta-blockers (metoprolol) affects patients with a heart attack (STEMI) who are in the cardiac intensive care unit. When patients are admitted to the unit, they will be randomly placed in one of two groups. One group will get the metoprolol medication, and the other will receive a placebo (a harmless pill that looks like the real medication). All other treatments will be the same for both groups. During the study, which is 72 hours long, patients will be monitored for blood pressure, heart rate, and lactate levels alterations. The main goal is to see if the medication helps improve patients condition or prevent it from getting worse. patients safety is a top priority, and if needed, the doctors can stop the study at any time if there are concerns.

This description comes directly from the study's public registry record.

Talk to the study team

Shir Frydman, MD  ·  0544267898  ·  shirfrydman@gmail.com

Yishay Szekely, MD  ·  yishay.szekely@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tel Aviv Sourasky Medical centerTel Aviv, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06967194