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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02048475
Other study ID # Kotoe _ 2
Secondary ID 2009-014620-36
Status Withdrawn
Phase Phase 4
First received October 8, 2013
Last updated November 24, 2014
Start date January 2010
Est. completion date February 2010

Study information

Verified date November 2014
Source Tampere University Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Finnish Medicines Agency
Study type Interventional

Clinical Trial Summary

To study the behavior of EEG during changing desflurane concentrations.


Description:

The concentration of desflurane will be increased to burst suppression EEG level, and thereafter decreased.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 2010
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- adult patients

Exclusion Criteria:

- pediatric patients

Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
desflurane
changing concentration

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary The behavior of EEG indices numbers during the course of anesthesia, with comparison to raw EEG traces How do the EEG indices reflect the clinical evaluation of anesthetic state and the visual appearance of EEG participants will be followed for the duration of surgical anesthesia, an expected average of 1 hour No
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