Volume Optimisation and Cognitive Function in Major Abdominal Surgery

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

October 1, 2017

Primary Completion Date

June 1, 2019

Study Completion Date

August 1, 2019

Conditions
Cognitive Decline
Interventions
DEVICE

multimodal monitoring

LiDCO Rapid, unilateral INVOS and unilateral BIS monitors will be applied. Should there be pre-existing carotid stenosis, INVOS sensor will be applied on the same side. In case of pre-existing cerebral pathology, the INVOS sensor will be applied to the contralateral side. Baseline values of nominal stroke index (SI), cardiac index (CI), BIS, mean arterial pressure (MAP) and regional oxygen saturation (rSO2) will be recorded. Basal rSO2 will be recorded prior to preoxygenation which raises the value. • Before the induction, up to 250ml of balanced crystalloid solution will be administered. These will include antibiotics solvents and other pre-induction i.v. therapy.

DEVICE

placebo

Before the induction, up to 250ml of balanced crystalloid solution will be administered. These will include antibiotics solvents and other pre-induction i.v. therapy.

Trial Locations (1)

1000

University Medical Centre, Ljubljana

All Listed Sponsors
lead

University Medical Centre Ljubljana

OTHER

NCT03186846 - Volume Optimisation and Cognitive Function in Major Abdominal Surgery | Biotech Hunter | Biotech Hunter