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Intraoperative Protective Ventilation and Postoperative Pulmonary Complications

NCT02671721 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-02-08

No results posted yet for this study

Summary

The purpose of this pilot study is to identify the optimal way to ventilate patients during abdominal surgery in order to reduce the amount of post-operative pulmonary complications in patients at moderate and high-risk for them.

Conditions

  • Complication of Ventilation Therapy
  • Postoperative Respiratory Complications

Interventions

OTHER

Maximal Compliance

PEEP will be set at the maximum static respiratory system compliance during a descending PEEP titration curve.

OTHER

Transpulmonary Pressure

We will use transpulmonary pressure values obtained using an naso/orogastric tube during the operative procedure to titrate PEEP intraoperatively.

Sponsors & Collaborators

  • Mayo Clinic

    collaborator OTHER

  • University of Colorado, Denver

    collaborator OTHER

  • Massachusetts General Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2017-03-31
Completion
2017-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT02671721 on ClinicalTrials.gov