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N/A
30 Years
75 Years
Not Enrolling
Both
Lung Cancer

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Trial Information


Inclusion Criteria:



- ASA physical status class I,II

- Unilateral lung lobectomy

- Use of one-lung ventilation

Exclusion Criteria:

- COPD

- CAOD

- Unstable cardiovascular status

- Peak inspiratory pressure > 30 mmHg

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor)

Outcome Measure:

arterial oxygenation

Outcome Description:

T1,T2,T3,T4: all measurement in lateral position, T1-arterial oxygenation(PaO2), T2-arterial oxygenation(PaO2),T3-arterial oxygenation(PaO2),T4-arterial oxygenation(PaO2)

Outcome Time Frame:

T1(10min before one-lung ventilation),T2(30min after one-lung ventilation),T3(60min), T4(10min after two lung ventilation)

Safety Issue:

Yes

Principal Investigator

Young Jun Oh, M.D.,PhD.

Investigator Role:

Study Chair

Investigator Affiliation:

Yonsei University College of Medicine

Authority:

Korea: Food and Drug Administration

Study ID:

1-2011-0027

NCT ID:

NCT01636973

Start Date:

March 2011

Completion Date:

April 2012

Related Keywords:

  • Lung Cancer
  • Lung cancer
  • Lung Neoplasms

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