Prevention of Pneumonia Comparing Ceftriaxone With Subglottic Aspiration

NCT00374959 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2006-09-26

No results posted yet for this study

Summary

The primary purpose of the trial is to compare the efficacy and safety of two measures which claim to prevent early-onset ventilator-associated pneumonia.

Conditions

Interventions

DEVICE

Endotracheal tube for aspiration of subglottic secretions.

Sponsors & Collaborators

  • Hoffmann-La Roche

    collaborator INDUSTRY
  • Hospital Universitario Principe de Asturias

    lead OTHER

Principal Investigators

  • Miguel Sanchez, MD, PhD · Hospital Universitario Principe de Asturias

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-10-31
Completion
2003-10-31

Countries

  • Spain

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 NCT00374959 on ClinicalTrials.gov