Comparison of esCCO calibration before and after anesthesia introductio

Not Applicable

Recruiting

• Conditions: Patients who undergo general anesthesia

• Registration Number: JPRN-UMIN000040626
• Lead Sponsor: BE Kohsan Central Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-03
• Last Update Posted: 17 October 2023
• Study Completion: 2026-03-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 330

Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients who are recognized as "patients who have difficulty in anesthesia" defined in the medical treatment fee score table L008 in the preoperative consultation 2) Patients with the following findings of arrhythmia confirmed by preoperative consultation i) Supraventricular rhythm irregularity such as atrial fibrillation, atrial flutter, sinus arrhythmia ii) bigeminal or trigeminal pulse iii) 2nd degree AV block, 3rd degree AV block 3) Patients who need pacing during surgery 4) Patients who need repositioning during surgery 5) Patients with cardiac tamponade 6) Patients who have undergone cardiopulmonary bypass surgery 7) Patients who have undergone artificial vascular replacement surgery 8) Patients undergoing emergency surgery 9) Patients who are judged to be inappropriate for this study by the investigator

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
esCCO measured before and afer anesthesia induction calibrated before anesthesia induction. And esCCO calibrated after anesthesia induction.