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Protective Ventilation During Pulmonary Lobectomy

NCT03174743 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2017-06-06

No results posted yet for this study

Summary

The investigator will evaluate the influence of lung protective ventilation on postoperative clinical outcome in patients undergoing one-lung ventilation for pulmonary lobectomy.

Conditions

Interventions

PROCEDURE

Convential Ventilation 1

High tidal volume, moderate inspired oygen fraction (FiO2).

PROCEDURE

Convential Ventilation 2

High tidal volume, high inspired oygen fraction (FiO2).

PROCEDURE

Protective Ventilation 1

Low tidal volume, PEEP, moderate inspired oygen fraction (FiO2) and recruitment maneuver.

PROCEDURE

Protective Ventilation 2

Low tidal volume, PEEP, High inspired oygen fraction (FiO2) and recruitment maneuver.

Sponsors & Collaborators

  • Xuzhou Medical University

    lead OTHER

Principal Investigators

  • Liu Su Liu, M.D/Ph.D · 徐州医科大学附属医院医学

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-02
Primary Completion
2018-06-01
Completion
2018-07-01

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03174743 on ClinicalTrials.gov