Clinical Trials Directory

Trials / Completed

CompletedNCT03576261

Heart Failure and Hemodynamic Stability During Anesthesia Induction

Does Heart Failure Has Impact on Hemodynamic Stability During Anesthesia Induction

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

Summary

The study aim is to investigate whether preoperative heart failure has impact on hemodynamic stability during anesthesia induction by target controlled infusion of anesthesia (TCI) in non-cardiac, non-morbidly obese surgery.

Detailed description

40 individuals are enrolled to the study after signed informed consent at the day of surgery. The study participants are randomized (non-blinded) to preoperative fluid therapy (preoperative colloid fluid bolus at 6 ml/kg LBW, Gelofusine™, Fresenius Kabi AB, Sweden) or control (no preoperative fluids) before standardized TCI- induction of anesthesia. No other intravenous fluids before anesthesia induction. Preoperative screening of biventricular systolic and diastolic function of the heart and level of venous return is implemented by transthoracic echocardiography approximately one hour before preoperative fluid therapy and anesthesia induction.

Conditions

Interventions

TypeNameDescription
OTHERPreoperative colloid fluid bolus (Gelofusine)Preoperative colloid fluid bolus
DIAGNOSTIC_TESTPreoperative transthoracic echocardiographyScreening of biventricular systolic and diastolic function of the heart and level of venous return by transthoracic echocardiography approximately one hour before preoperative fluid therapy and anesthesia induction.

Timeline

Start date
2018-08-01
Primary completion
2021-12-01
Completion
2021-12-02
First posted
2018-07-03
Last updated
2021-12-16

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT03576261. Inclusion in this directory is not an endorsement.