Hepatectomy Clinical Trial
Official title:
Prospective, Randomized, Simple Blind Study Comparing the Effects of an Anaesthesia With Propofol to an Anaesthesia With Desflurane on Oxydative Stress and Liver Function Recovery After Hepatectomy
Propofol is an anaesthetic agent that showed in vitro and in vivo anti oxidant properties.
No data are available concerning the potential benefit of a total anaesthesia with propofol
in partial hepatic surgery. Patients who undergo partial hepatic resection have frequent
liver insufficiency that could be related in part to the oxidative stress induced by
clamping the hepatic vessels during the surgical intervention. Our hypothesis is that
propofol, by increasing liver resistance to this ischemia-reperfusion phenomenon, could
improve the remaining liver function recovery, and therefore could reduce post surgical
morbidity.
The aim of the study is to evaluate the anti oxidant effects of propofol compared to another
widely used anaesthetic agent, inhaled desflurane, during and after partial hepatic
resection with hepatic vessels clamping. The primary endpoint will be the level of
malondialdehyde (a plasmatic marker of oxidative stress), 30 minutes after the end of
hepatic clamping.
Propofol is an anaesthetic agent that showed in vitro and in vivo anti oxidant properties.
No data are available concerning the potential benefit of a total anaesthesia with propofol
in partial hepatic surgery. Patients who undergo partial hepatic resection have frequent
liver insufficiency that could be related in part to the oxidative stress induced by
clamping the hepatic hilum during the surgical intervention. Our hypothesis is that
propofol, by increasing liver resistance to ischemic-reperfusion injury, could improve the
remaining liver function recovery, and therefore could reduce post surgical morbidity.
The aim of the study is to evaluate the anti oxidant effects of propofol compared to another
widely used anaesthetic agent, inhaled desflurane, during and after partial hepatic
resection with hepatic hilum clamping.
The primary endpoint will be the level of malondialdehyde (a plasmatic marker of oxidative
stress), 30 minutes after the end of hepatic clamping.
The evolution over time of other markers of oxidative stress will be studied (glutathione,
myeloperoxidase, nitric oxide), as well as functional and biological markers of liver
regeneration.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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