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NCT03360955 Clinical Trial

Comparison of Extubation Time Between Total Intravenous Anesthesia With Spinal Anesthesia for Cardiac Surgery

Anesthesia Clinical Trial

Official title:
Comparison of Extubation Time Between Total Intravenous Anesthesia Guided by Bispectral Index With Spinal Anesthesia With Minimal Opioid Dose for Cardiac Surgery

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03360955
Other study ID # R-2017-3604-40
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 13, 2017
Est. completion date December 2021

Study information
Verified date August 2020
Source Coordinación de Investigación en Salud, Mexico
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study compares the extubation time between total intravenous anesthesia guided by Bispectral Index with spinal anesthesia with minimal opioid dose for cardiac surgery.

Description:

This study compares the time needed to extubate of two anesthesic techniques, 1) Total Intravenous Anesthesia guided by Bispectral Index (BIS), 2) Spinal Anesthesia with minimal opioid dose for cardiac surgery.

Identify the best anesthesia technique to do ultrafast track extubation can minimize the risk of infection associated.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 60
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

Patients scheduled for cardiac surgery Physical Status Classification System of the American Society of Anesthesiologists (ASA) II-III

Exclusion Criteria:

Physical Status Classification System of the American Society of Anesthesiologists (ASA) IV-V Emergency cardiac surgery Spinal defect

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Anesthesia
Different anesthesia technique will be compared to find out which one offers better outcome to perform ultrafast track extubation

Locations
Country Name City State
Mexico Hospital de cardiología Ciudad de mexico Cdmx

Sponsors (1)
Lead Sponsor Collaborator
Coordinación de Investigación en Salud, Mexico

Country where clinical trial is conducted

Mexico, 

Outcome
Type Measure Description Time frame Safety issue
Primary Extubation time The time from anesthesia emergence to extubation will be measured in minutes Up to 1 hour after anesthesia emergence
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