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Clinical Trials/NCT01448811
NCT01448811
Completed
Not Applicable

Impact of Auditory Evoked Potential Index Monitoring on Bronchoscopic Examination in the Mechanical Ventilated Patients - A Prospective, Randomized, Controlled Study

Kaohsiung Veterans General Hospital.1 site in 1 country37 target enrollmentMarch 2007
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ConditionsSedation Method

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sedation Method
Sponsor
Kaohsiung Veterans General Hospital.
Enrollment
37
Locations
1
Primary Endpoint
Change of mean arterial pressure, heart rate and AAI
Status
Completed
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

To compare the difference of sedation monitoring for bronchoscopic examination monitoring by auditory evoked potentials (AEP) or Ramsay Sedation Scale (RSS) in mechanical ventilated patients.

Registry
clinicaltrials.gov
Start Date
March 2007
End Date
March 2008
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Chien-Wei Hsu

Assisted Professor

Kaohsiung Veterans General Hospital.

Eligibility Criteria

Inclusion Criteria

  • •Mechanically ventilated patients with aged 18 or over and they needed bronchoscopic examination in the ICU were eligible for this study.

Exclusion Criteria

  • •patients with pacemaker, neuromuscular blockades, propofol allergy or hearing impairment.

Outcomes

Primary Outcomes

Change of mean arterial pressure, heart rate and AAI

Time Frame: 40 minutes

During bronchoscopy, we recorded AAI number, blood pressure and heart rate every 5 minutes, totally up to 40 minutes.

Secondary Outcomes

  • mean propofol dose use during examination, times of propofol dose adjustment(40 minutes)

Study Sites (1)

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