The purpose of the study is to assess feasibility of future large randomised controled study aimed on assessment of effect of goal-directed therapy on incidence of complications in neurosurgery compared to standard care.
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Serious Adverse Events 1
Timeframe: During the Surgery
Serious Adverse Events 2
Timeframe: 24 hours postoperatively
Recruitment rate
Timeframe: through study completion, an average of 6 months
Completeness of Case Report Forms
Timeframe: through study completion, an average of 6 months