NCT03358680CompletedNot Applicable
Temperature and Analgesia Monitoring During Cardial Parmonary Bypass
China International Neuroscience Institution1 site in 1 country39 target enrollmentStarted: May 1, 2017Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 39
- Locations
- 1
- Primary Endpoint
- IOC2
Study Overview
Brief Summary
- Investigator will apply IOC2 to reflect the depth of analgesic during hypothermia in CPB period.
- effectiveness of IOC2 monitoring for anesthetic depth versus commonly used vital sign monitoring based on factors such as blood pressure and heart rate.
- Evaluate the other sedation co-relation measurement, include BIS , IOC2 to reflected the consciousness during the operation.
- Evaluate the other hemodynamic index, include CO, SVV, CVP, PPV to reflect the circulation function , and the effect to the IOC2 and IOC1.
- Describe the trend of all the measurement. detect the variation of the index during the temperature change during the CPB.
Detailed Description
In this study,
- Investigator will apply IOC2 to reflect the depth of analgesic during hypothermia in CPB period.
- Furthermore, investigator evaluated the effectiveness of IOC2 monitoring for anesthetic depth versus commonly used vital sign monitoring based on factors such as blood pressure and heart rate.
- Evaluate the other sedation co-relation measurement, include BIS , IOC2 to reflected the consciousness during the operation.
- Evaluate the other hemodynamic index, include CO, SVV, CVP, PPV to reflect the circulation function , and the effect to the IOC2 and IOC1.
- Describe the trend of all the measurement. detect the variation of the index during the temperature change during the CPB.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •undergoing coronary artery bypass surgery
Exclusion Criteria
- •change the surgery planning during the operation
Outcomes
Primary Outcomes
IOC2
Time Frame: 1 DAY
Index of consciousness 2
Secondary Outcomes
- BIS(1 DAY)
- IOC1(1 DAY)
Investigators
Study Sites (1)
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