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Intraoperative Protective Ventilation in Abdominal Surgery (IMPROVE Study)

NCT01282996 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2012-10-05

No results posted yet for this study

Summary

The purpose of this study is to compare the influence of a lung protective ventilation with conventional ventilation on postoperative complications following major abdominal surgery.

Conditions

  • Protective Lung Ventilation Using:
  • Low Tidal Volume (6-8 mL/kg Predicted Body Weight)
  • PEEP of 6-8 cmH2O
  • Intraoperative RMs

Interventions

OTHER

Abdominal surgery

to compare the influence of a lung protective ventilation with conventional ventilation on postoperative complications following major abdominal surgery

Sponsors & Collaborators

  • University Hospital, Clermont-Ferrand

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2012-08-31
Completion
2012-08-31

Countries

  • France

Study Locations

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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 NCT01282996 on ClinicalTrials.gov