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Effect of Nitrous Oxide on Intravenous Closed-loop Anesthesia

NCT00547209 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 672

Last updated 2016-09-26

No results posted yet for this study

Summary

The main objective of the study is to analyze the influence of nitrous oxide on propofol and remifentanil requirements.

Conditions

  • Anesthesia

Interventions

DRUG

air

60% air combined with 40% oxygen for ventilation

DRUG

Nitrous oxide

60% nitrous oxide combined with 40% oxygen for ventilation

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Principal Investigators

  • Marc Fischler, MD · Hopital Foch, 92150 Suresnes, France

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2009-11-30
Completion
2009-11-30

Countries

  • Belgium
  • France
  • Germany

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 NCT00547209 on ClinicalTrials.gov