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The prophylactic effect of continuously infused landiolol started just before the end of surgery against tachycardia during tracheal extubatio

Phase 4
Conditions
Patients undergoing a surgery with general anesthesia
Registration Number
JPRN-UMIN000004648
Lead Sponsor
Bellland General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
45
Inclusion Criteria

Not provided

Exclusion Criteria

patients with chronic heart failure, atrio-ventricular block, sick-sinus syndrome, diabetic ketoacidosis, hypothyroidism, WPW syndrome, hypotention (systric and diastric blood pressure should be more than 90 and 60, respectively), bradycardia (HR < 50), recieved nicardipine treatment for hypertention with extubation, asthma, with beta-blocker treatment, with anaphylaxis for flurbiprofen, with pregnancy, with anaphylaxis for landiolol, judged as unsuitable for this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the maximum heart rate during tracheal extubation
Secondary Outcome Measures
NameTimeMethod
age, height, body weight, sex, preoperative complications blood pressure and heart rate (at starting infusion of landiolol, 10 min after starting infusion of landiolol, maximum heart rate during tracheal extubation, after tracheal extubation, at discharging the patient from operating room) operative time, anesthetic time, total fluid infusion, total operative bleeding, total volume of urine, total transfusion total dose of fentanyl, total dose of remifentanil, total dose of landiolol the incidence of side effect (bradycardia etc.)
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