Effect of Anesthetics on Oxygenation and Microcirculation During One-lung Ventilation

Sponsor
Seoul National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02191371
Collaborator
(none)
104
1
2
5
20.7

Study Details

Study Description

Brief Summary

One-lung ventilation during thoracic surgery may affect systemic oxygenation and peripheral microcirculation by hypoxic pulmonary vasoconstriction. Both intravenous and inhalational anesthetics can be used during one-lung ventilation. However, there is still a controversy which anesthetic would be more appropriate during one-lung ventilation in the perspective of oxygenation and microcirculation. The investigators hypothesized that intravenous and inhalational anesthetics may affect oxygenation and microcirculation differently during one-lung ventilation.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Patients undergoing thoracic surgery including one-lung ventilation will be randomized to receive intravenous (propofol) or inhalational (desflurane) anesthetic.

Systemic oxygenation can be evaluated by measuring partial pressure of oxygen in arterial blood analysis. Microcirculatory parameters can be obtained from vascular occlusion test. Among those parameters, recovery slope during vascular occlusion test is known to reflect recruitment of microvasculature in response to hypoxic or ischemic insult. In this study, we will compare arterial partial pressure of oxygen and recovery slope during one-lung ventilation between propofol and desflurane group.

Study Design

Study Type:
Interventional
Actual Enrollment :
104 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Effect of Anesthetics on Oxygenation and Microcirculation During One-lung Ventilation
Study Start Date :
Jul 1, 2014
Actual Primary Completion Date :
Dec 1, 2014
Actual Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: propofol

Propofol is used as a maintenance anesthetic to patients in the propofol group. Intervention: propofol infusion by target-controlled infusion for maintaining anesthesia propofol (Fresofol MCT 2%) target effect site concentration: 4~5 mcg/ml, during general anesthesia

Drug: propofol
Patients are randomized to receive intravenous anesthetic (propofol) or inhalational anesthetic (desflurane) as a maintenance anesthetic.
Other Names:
  • propofol (Fresofol(R)2 MCT 2%, Fresenius Kabi)
  • Experimental: desflurane

    Desflurane is used as a maintenance anesthetic to patients in the desflurane group. Intervention: Desflurane administration for maintaining anesthesia desflurane (Suprane) inhalation as 6~8 vol% during general anesthesia

    Drug: desflurane
    Patients are randomized to receive intravenous anesthetic (propofol) or inhalational anesthetic (desflurane) as a maintenance anesthetic.
    Other Names:
  • desflurane (Suprane(R), Baxter Healthcare)
  • Outcome Measures

    Primary Outcome Measures

    1. arterial partial pressure of oxygen [30 min after one-lung ventilation]

      Primary outcome is arterial partial pressure of oxygen 30 min after one-lung ventilation during thoracic surgery in propofol and desflurane groups.

    Secondary Outcome Measures

    1. recovery slope [30 min after one-lung ventilation]

      Secondary outcome is recovery slope measured by vascular occlusion test 30 min after one-lung ventilation during thoracic surgery in propofol and desflurane groups.

    Other Outcome Measures

    1. blood pressure [30 min after one-lung ventilation]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • undergoing thoracic surgery including one-lung ventilation
    Exclusion Criteria:
    • refuse to enroll

    • BMI over 30 kg/m(2)

    • severe obstructive or restrictive lung disease

    • preoperative supplemental oxygen, intubated, or mechanical ventilatory support

    • preoperative arterial partial pressure of oxygen < 60 mmHg

    • pregnancy

    • history of coronary artery disease

    • preoperative continuous infusion of vasopressor or inotropes

    • cannot undergo vascular occlusion test: anatomical abnormality of both arms, severe peripheral vascular disease, presence of A-V fistula

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Hospital Seoul Korea, Republic of 110-744

    Sponsors and Collaborators

    • Seoul National University Hospital

    Investigators

    • Principal Investigator: Yunseok Jeon, PhD, Seoul National University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT02191371
    Other Study ID Numbers:
    • PaO2 & StO2 in OLV
    First Posted:
    Jul 16, 2014
    Last Update Posted:
    Oct 13, 2016
    Last Verified:
    Aug 1, 2014
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Seoul National University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 13, 2016