Phase
Condition
Chest Pain
Coronary Artery Disease
Thrombosis
Treatment
N/AClinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Being older than 18 but, not older than 75
Scheduled for surgery under general anesthesia
Duration of surgery scheduled as 2 hours or longer
Exclusion
Exclusion Criteria:
Intracranial or intrathoracic surgery (due to difficulty using a BIS monitor orfrequent need for beta-receptor antagonism)
Indication for perioperative beta-receptor antagonism
Current use of calcium-channel antagonists
History of coronary artery disease
History of reactive airway disease
History of diabetes or other disorders of glucose metabolism
Reported allergy to any of the study drugs
Reported substance abuse (except nicotine and caffeine)
Use of monoamine oxidase (MAO) inhibitor drugs
Hypersensitivity to metoprolol, esmolol and related derivatives, or to any of theexcipients of either.
Hypersensitivity to other beta-blockers (cross-sensitivity between beta-blockers canoccur).
Sick-sinus Syndrome.
Heart block greater than first degree, cardiogenic shock, and overt cardiac failure.
Significant first-degree heart block (P-R interval greater than or equal to 0.24 sec;systolic pressure < 100mmHg; or moderate- to-severe cardiac failure).
Severe peripheral arterial circulatory disorders.
Pheochromocytoma.
Baseline heart rate of < 60
Systolic pressure less than 100 mm Hg
Pregnant women
Prisoners
Study Design
Study Description
Connect with a study center
Univeristy of Oklahoma Health Sciences Center Dept. Anesthesiology
Oklahoma, Oklahoma 73104
United StatesSite Not Available
Univeristy of Oklahoma Health Sciences Center Dept. Anesthesiology
Oklahoma City, Oklahoma 73104
United StatesSite Not Available

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