Clinical Trials Directory

Trials / Completed

CompletedNCT01811966

Preoperative Volume Substitution in Elective Surgery Patients

Preoperative Volume Substitution in Fasting Patients Undergoing Elective Surgery - Impact on Hemodynamic Stability During Anesthesia

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

Summary

Preoperative fasting can evoke a hypovolemia which may cause a hemodynamic instability during introduction of anesthesia. The purpose of this study is to test the hypothesis that a defined preoperative volume substitution compared to standard procedure will result in a reduced incidence of hemodynamic instabilities during introduction of anesthesia in elective surgery patients.

Detailed description

The preoperative fasting period often lasts longer than 2 hours as recommended by various national and international anesthetic guidelines. Thus, hypovolemia is more often then anticipated. In awake patients this condition is often masked. Introduction of anesthesia often leads to an unmasking of hypovolemia with a consecutive hemodynamic instability. Aim of the study is to test the hypothesis that a preoperative volume substitution (8 ml/kg RingerAcetate Solution in 15 min. prior to introduction of anesthesia) reduces possible hemodynamic instabilities during initiation of anesthesia.

Conditions

Interventions

TypeNameDescription
OTHERVolume
OTHERControl

Timeline

Start date
2013-03-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2013-03-15
Last updated
2015-07-29

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01811966. Inclusion in this directory is not an endorsement.