Trial Information
The EC90 of Remifentanil Blunting Hemodynamic Changes to Head Fixation in the Patients Undergoing Neurosurgery
Inclusion Criteria:
- patients undergoing neurosurgery that require head fixation with mayfield head holder
- patients who agree to our study
Exclusion Criteria:
- patients who don't agree to our study
- BMI<16.0 or BMI>30
- cardiovascular disease, pulmonary disease, renal disease
- alcoholic abuser or drug abuser
- patients who takes any drug having an influence on cardiovascular system or
sympathetic nervous system
- any use of local anesthetics or drugs which have an influence on cardiovascular
system from beginning of induction to peri-fixation period
Type of Study:
Interventional
Study Design:
Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Outcome Measure:
mean arterial blood pressure
Outcome Description:
mean arterial blood pressure will be recorded at 2 minutes before fixation, 1 minute before fixation, highest value during immediately post-fixation periord, 1 minute after fixation, 2 minutes after fixation, 3 minutes after fixation, 4 minutes after fixation and 5 minutes after fixation.
Outcome Time Frame:
peri-fixation periord
Safety Issue:
No
Authority:
Korea: Food and Drug Administration
Study ID:
JHBahk_fixation_remifentanil
NCT ID:
NCT01489137
Start Date:
November 2011
Completion Date:
Related Keywords:
- Brain Tumor
- AVM
- ICH
- Brain Neoplasms