Comparison of Humidification Devices During Non Invasive Ventilation, in Acute Respiratory Failure

NCT00190346 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2011-10-26

No results posted yet for this study

Summary

Comparison of humidification devices during non invasive ventilation, in acute respiratory failure.

The hypothesis was, due to dead space, lower humidification, a reduced efficiency of the technique (NIV) when HME are used in comparison with HH.

Conditions

Interventions

DEVICE

Humidification devices: HH vs HME

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Nicolas Best · DRRC hopitaux de Paris

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2001-12-31
Completion
2003-04-30

Countries

  • Canada
  • France
  • Italy
  • Tunisia

Study Locations

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Entities

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 NCT00190346 on ClinicalTrials.gov