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Beta-blocker Before Extubation

Use of Prophylactic Beta Blockade to Prevent Peri-extubation Cardiac Ischemia and Congestive Heart Failure

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00563238
Enrollment
0
Registered
2007-11-26
Start date
2007-11-30
Completion date
2009-12-31
Last updated
2017-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Ischemia

Keywords

Extubation

Brief summary

Silent myocardial ischemia is known to occur in the general medical intensive care unit population immediately following tracheal extubation. We believe these patients are at risk for primary cardiac events in the 4 hours immediately following extubation. Metoprolol is a selective beta-1 antagonist, with little to no beta-2 activity at low and moderate doses. The cardioprotective effects of beta blockade have been well documented in randomized controlled trials. In patients undergoing extubation, prophylactic use of intravenous metoprolol may reduce post-extubation ischemia events as well as precursors of cardiogenic pulmonary edema (atrial and ventricular wall tension). Our primary hypothesis is that prophylactic metoprolol (titrated to reduce resting heart rate by at least 10%) prior to tracheal extubation will reduce the rate of ischemia as judged by ST segment analysis.

Interventions

DRUGMetoprolol

Metoprolol administered intravenously in 2.5mg boluses until the resting heart rate falls by 10% from baseline to a maximum dose of 10mg, or until there is any apparent adverse reaction.

Sponsors

Gregory A. Schmidt
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Adult medical or cardiac intensive care unit patients on mechanical ventilation who have known coronary artery disease or have at least 2 of the following risk factors for coronary artery disease: * Cigarette smoking * Hypertension (BP 140/90 or antihypertensive medication) * Low HDL-cholesterol (HDL-C) (\<40 mg/dL \[1.03 mmol/L\]) * Family history of premature CHD (in male first degree relatives \<55 years, in female first degree relative \<65 years) * Age (men 45 years, women 55 years) * Diabetes mellitus * Symptomatic carotid artery disease * Peripheral arterial disease * Abdominal aortic aneurysm

Exclusion criteria

* Arterial hypotension, defined as mean arterial pressure \< 60 mmHg or requiring any intravenous vasoactive medication. * The presence of known reactive airway disease. * Resting heart rate of \<60 in the period prior to tracheal extubation.. * The presence of decompensated congestive heart failure, defined as requiring continuous infusion of an inotropic agent. * Known hypersensitivity to beta-blockers or any other contraindication to their use. * Subjects younger than 18 years of age. * Inability to obtain consent from the subject or the subjects authorized representative. * Pregnancy * Digoxin therapy * Current therapy with a beta-blocker

Design outcomes

Primary

MeasureTime frame
The rate of ischemia as judged by ST segment analysis in the 4h following extubation4 hours

Secondary

MeasureTime frame
Rate-pressure product following extubation30min, 2h, 4h
Troponin T elevations, the incidence of cardiogenic edema, and the rate of reintubation48h
Pro-BNP levels30min

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026