Registry of Cardio/Neurovascular Anesthesia Including the Database of Biological Signals During Anesthesia, Preoperative Assessment and Prognosis in Patients

Overview

Monitoring data during anesthesia of cardio/neurovascular surgical patient in the operation room or hybrid room would be collected and stored into the registry automatically. Patients' information, preoperative assessment and patients' short-term/long-term prognosis from medical records would be included in the registry. Intraoperative data including I/O balance, events and the use of vasoactive medications would also be included in the registry. The purpose of the registry is to establish an automatically collected and accessible database of cardio/neurovascular surgical patients for further retrospective studies.

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: December 31, 2022

Arms, Groups and Cohorts

  • Anesthesia for cardio/neurovascular surgery or procedure
    • Patients undergoing anesthesia in an operating room or hybrid room for cardio/neurovascular surgery or procedure.

Clinical Trial Outcome Measures

Primary Measures

  • heart rate in bpm
    • Time Frame: During the surgery or procedure
  • systemic/pulmonary arterial blood pressure in mmHg
    • Time Frame: During the surgery or procedure
  • central venous pressure in mmHg
    • Time Frame: During the surgery or procedure
  • oxygen saturation in %
    • Time Frame: During the surgery or procedure
  • body temperature in degrees celsius
    • Time Frame: During the surgery or procedure
  • respiratory parameters -(airway pressure in cmH2O
    • Time Frame: During the surgery or procedure
  • respiratory parameters -fraction of inspired O2 in %
    • Time Frame: During the surgery or procedure
  • respiratory parameters -end-tidal concentration of volatile anesthetics in %
    • Time Frame: During the surgery or procedure
  • respiratory parameters -end-tidal CO2 in mmHg)
    • Time Frame: During the surgery or procedure
  • EEG-based monitoring of general anesthesia (in Bispectral index or Patient state index)
    • Time Frame: During the surgery or procedure
  • cerebral oxygen concentration in %
    • Time Frame: During the surgery or procedure
  • infusion history of target-controlled infusion pump in cc/h or effect site concentration (Ce)
    • Time Frame: During the surgery or procedure
  • cardiac output in l/min
    • Time Frame: During the surgery or procedure

Participating in This Clinical Trial

Inclusion Criteria

1. Patients scheduled to undergo anesthesia for cardio/neurovascular surgery or procedure 2. Adults over 19 years of age Exclusion Criteria:

1. Emergency situation in which there is not enough time to decide whether the patients will participate in this study (transfer to operation/hybrid room within 1 hour of visit)

Gender Eligibility: All

Minimum Age: 19 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Yonsei University
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Sarah Soh, MD, PhD, Principal Investigator, Department of Anesthesiology and Pain Medicine, Yonsei Cardiovascular Hospital, Yonsei University College of Medicine
  • Overall Contact(s)
    • Sarah Soh, MD, PhD, 82-2-2228-8512, yeonchoo@yuhs.ac

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