Clinical Trials Directory

Trials / Terminated

TerminatedNCT01594021

Efficacy of Preemptive Volume Loading to Prevent Arterial Hypotension During Induction of General Anesthesia

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
17 (actual)
Sponsor
Hopital Foch · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Induction of general anesthesia induces frequently arterial hypotension. The short term goal of this study is to evaluate if preemptive volume loading prevents such complication.

Detailed description

This is a randomized, prospective study which will include a total of 200 patients who are scheduled to undergo elective surgery. The research participants will be randomly assigned to * a control group that will receive a low preemptive volume loading (50 mL of gelatin), * a protocol group that will receive a high preemptive volume loading (500 mL of gelatin). Volume loading is preceded by the measurement of stroke volume and cardiac output before and after a passive leg elevation test and followed by a standardized anesthetic protocol.

Conditions

Interventions

TypeNameDescription
DRUGGelatin 500 mLintravenous administration
DRUGGelatin 50 mLintravenous administration

Timeline

Start date
2012-07-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2012-05-08
Last updated
2016-10-31

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01594021. Inclusion in this directory is not an endorsement.