Anesthesia Clinical Trial
Official title:
Measurement of the Second Gas Effect on Sevoflurane in Anaesthetised Patients
This study is investigating the "second gas effect", a phenomenon produced by the uptake of nitrous oxide (N2O) by the lungs, during the course of a typical anaesthetic. The effect is to increase the concentration of other breathed gases in the lung. These include oxygen and volatile anaesthetic agents such as sevoflurane, which are also normally administered along with N2O. We wish to i) measure the magnitude of the second gas effects on both blood and expired concentrations of sevoflurane (Part 1), and ii) see if a demonstrable difference exists between the effects on blood and expired concentrations.
This study is investigating the "second gas effect", a phenomenon produced by the uptake of
nitrous oxide (N2O) by the lungs, during the course of a typical anaesthetic. The effect is
to increase the concentration of other breathed gases in the lung. These include oxygen and
volatile anaesthetic agents such as sevoflurane, which are also normally administered along
with N2O.
While the second gas effect has been demonstrated previously, by measuring the concentration
of volatile anaesthetic in the expired breath, no study has yet shown that it has a
significant effect on the concentrations in the blood. The blood concentration is in fact
more important, as it directly determines the concentration of anaesthetic reaching the
brain, and therefore the effect on the depth of anaesthesia. The second gas effect on blood
concentrations may be more powerful than that on expired concentrations, due to the
detrimental effect of anaesthesia on the evenness of distribution of ventilation and blood
flow in the lung.
The proposed study will have two parallel components or Parts. We wish to i) measure the
magnitude of the second gas effects on both blood and expired concentrations of sevoflurane
(Part 1), and ii) see if a demonstrable difference exists between the effects on blood and
expired concentrations.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label
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