Clinical Trials Directory

Trials / Completed

CompletedNCT03394833

Hemodynamic Stability During Induction of Anaesthesia

Hemodynamic Stability During an Induction of Anaesthesia: A Randomized, Non-blinded Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Umeå University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study aim is to investigate if preoperative volume bolus based on lean body weight could preserve mean arterial pressure during target controlled infusion of anaesthesia (TCI) or rapid sequence induction of anaesthesia (RSI) in non-cardiac, non-morbidly obese surgery.

Detailed description

40 individuals are enrolled to TCI and RSI groups respectively. The randomization process for preoperative fluid bolus prior to induction of anaesthesia is conducted in respective group at the day of surgery. Preoperative colloid fluid therapy (6 ml/kg LBW, Gelofusine™, Fresenius Kabi Ab, Sweden) is infused rapidly before non-invasive baseline blood pressure (NIBP) measurements in twenty individuals in each group. No other intravenous fluids before induction of anaesthesia. NIBPs, pulse frequency, peripheral saturation (SpO2) are registered and collected 20 minutes post induction.

Conditions

Interventions

TypeNameDescription
OTHERgelofusinePreoperative colloid fluid bolus 6ml/kg ideal body weight

Timeline

Start date
2017-11-20
Primary completion
2018-12-15
Completion
2019-04-30
First posted
2018-01-09
Last updated
2019-09-26

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT03394833. Inclusion in this directory is not an endorsement.