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Search / Trial NCT00374959

Prevention of Pneumonia Comparing Ceftriaxone With Subglottic Aspiration

Launched by HOSPITAL UNIVERSITARIO PRINCIPE DE ASTURIAS · Sep 11, 2006

Trial Information

Current as of June 02, 2025

Completed

Keywords

Prevention Of Pneumonia Ceftriaxone Continuous Aspiration Subglottic Secretions Mechanical Ventilation With Endotracheal Intubation. Absence Of Infection

ClinConnect Summary

Background: In a previous double-blind, placebo-controlled, randomized trial we found that a 3-day-course of ceftriaxone significantly reduced the incidence of early-onset ventilator-associated pneumonia (EOP). Continuous aspiration of secretions accumulating in the subglottic space above the cuff of the endotracheal tube has also been shown to prevent EOP.

Objective: To compare the effect of both preventive measures on the incidence of EOP.

Design: Randomized, multicenter.

Setting: Three general intensive care units at university hospitals in Spain. Patients: Patients without signs of i...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Endotracheal intubation with endotracheal tube equipped with port for aspirations of subglottic contents and expected to exceed 48 hors.
  • Absence of infection.
  • 18 years or older.
  • Informed Consent.
  • Exclusion Criteria:
  • Endotracheal intubation prior to admission to hospital.
  • Allergic to beta-lactam antibiotics.
  • Formal indication for systemic antibiotic therapy.

About Hospital Universitario Principe De Asturias

Hospital Universitario Príncipe de Asturias is a leading healthcare institution in Spain, renowned for its commitment to advanced medical research and clinical excellence. As a prominent clinical trial sponsor, the hospital integrates cutting-edge scientific innovation with patient-centered care, facilitating a diverse range of clinical studies aimed at improving health outcomes. With a multidisciplinary team of experienced researchers and healthcare professionals, the hospital emphasizes ethical standards and regulatory compliance, ensuring the safety and welfare of trial participants while contributing to the advancement of medical knowledge and treatment options.

Locations

Alcala De Henares, Madrid, Spain

Getafe, Madrid, Spain

Barcelona, , Spain

Patients applied

0 patients applied

Trial Officials

Miguel Sanchez, MD, PhD

Principal Investigator

Hospital Universitario Principe de Asturias

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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