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Clinical Trial Summary

The purpose of this international multicenter, patient and outcome-assessor blinded randomized controlled trial is to determine whether the application of an individualized high PEEP strategy, aiming at avoiding an increase in the driving pressure during intraoperative ventilation, protects against the development of postoperative pulmonary complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Postoperative Respiratory Complication

NCT number NCT03884543
Study type Interventional
Source Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Contact Sunny Nijbroek, MD
Phone +3120-56 62533
Email s.g.nijbroek@amc.nl
Status Recruiting
Phase N/A
Start date April 23, 2019
Completion date March 2024

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Terminated NCT04732143 - Effect of Preoperative Incentive Spirometer on Postoperative Pulmonary Complications Following Lung Resection N/A