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Depth of Anesthesia in Cardiac Surgery

Monitoring of Anesthetic Depth During Surgical Correction of Acquired Valvular Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01524354
Enrollment
28
Registered
2012-02-01
Start date
2010-03-31
Completion date
2011-12-31
Last updated
2012-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Valve Diseases

Keywords

depth of anesthesia, valve surgery

Brief summary

The aim of our study was to evaluate the significance of monitoring anesthetic depth for the conduct of anesthesia and the early postoperative period in patients subjected to surgical correction of combined valvular disorders.

Detailed description

Our aim was to evaluate the effect of monitoring anesthetic depth on duration of postoperative mechanical ventilation and ICU stay after surgical correction of combined valvular disorders.

Interventions

intraoperative maintenance of anesthesia with propofol under control of cerebral state index at 40-60 points

Sponsors

Northern State Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* requirement of surgical correction of two or more valves

Exclusion criteria

* no

Design outcomes

Primary

MeasureTime frameDescription
duration of postoperative mechanical ventilation24 hours postoperativelyCriteria for termination of postoperative respiratory support were the following: patient able to cooperate; adequate muscular tone; SpO2 \> 95% with FiO2 0.5; PaCO2 \< 45 mm Hg; postoperative bleeding rate \< 50 mL hr-1; stable hemodynamics without inotropic/vasopressor support; body temperature of \> 35 °C. Temporary pacing was not regarded as a contraindication for tracheal extubation.

Secondary

MeasureTime frameDescription
length of ICU stay7 days postoperativelyThe time until 'fit for ICU discharge' criteria as well as the actual length of the ICU stay were registered. The 'fit for ICU discharge' criteria included the following: fully oriented patient, SaO2 \> 90% on room air, no episodes of severe arrhythmias, bleeding \< 50 mL hr-1, diuresis \> 0.5 mL kg-1 hr-1, no need for inotropic/vasopressor support and no signs of ischemia on ECG.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026