Estimating Blood Concentrations of Anaesthetics During One-Lung Ventilation (OLV)
NCT ID: NCT02821455
Last Updated: 2018-08-02
Study Results
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View full resultsBasic Information
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COMPLETED
19 participants
OBSERVATIONAL
2016-08-31
2017-01-31
Brief Summary
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Detailed Description
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Mechanically supporting the patient's breathing using only one of the two lungs, known as one-lung ventilation, is used in lung surgery to allow the surgeon to gain access to one side of the chest whilst the anaesthetist supports the lung on the other side. One-lung ventilation markedly alters the exchange of gases in the lungs, including anaesthetic gases. Because of this derangement, it is not known if the end-tidal concentrations are related to blood levels of anaesthetic gases during this type of mechanical ventilation. The aims of the study is to determine if end-tidal concentrations of anaesthetics as measured by a standard gas monitor are related to the blood levels of the gases isoflurane and sevoflurane during one-lung ventilation.
Patients over 18 years old undergoing planned lung surgery with one-lung ventilation and anaesthesia with isoflurane or sevoflurane, and who have a routine tube inserted into an artery in their wrist to monitor blood pressure will be recruited for the study. During the study, two blood samples the size of two teaspoons each will be taken from the tube in the artery and two end-tidal concentration recordings.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Lung Surgery with One-Lung Ventilation
A single cohort of patients undergoing one-lung ventilation during lung surgery
Lung Surgery with One-Lung Ventilation
A single cohort of patients undergoing one-lung ventilation during lung surgery
Interventions
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Lung Surgery with One-Lung Ventilation
A single cohort of patients undergoing one-lung ventilation during lung surgery
Eligibility Criteria
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Inclusion Criteria
* Admitted for elective thoracic surgery using one-lung ventilation obtained by the use of a double-lumen endotracheal tube or bronchial blocker.
* Elective surgery planned between 1 August and 30 November 2016
* Planned insertion of an arterial cannula by anaesthetist for routine monitoring of systemic arterial pressure
* Planned inhalational anaesthesia technique with isoflurane or sevoflurane.
* Patients who have provided consent to take part in the study
Exclusion Criteria
* History of malignant hyperthermia
* Emergency thoracic surgery
* Patients who have not consented to take part in the study
18 Years
ALL
No
Sponsors
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NHS Lothian
OTHER_GOV
University of Edinburgh
OTHER
Responsible Party
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Principal Investigators
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R P Alston, MBChB,FRCA
Role: PRINCIPAL_INVESTIGATOR
University of Edinburgh
Locations
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Royal Infirmary of Edinburgh
Edinburgh, , United Kingdom
Countries
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Other Identifiers
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AC16081
Identifier Type: -
Identifier Source: org_study_id
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