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Antibiotic Compound Coating

CeraShield Endotracheal Tube for Ventilator-Associated Pneumonia (CEASEVAP Trial)

N/A
Waitlist Available
Led By John MUSCEDERE, MD
Research Sponsored by Queen's University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Adult critically ill patients with respiratory failure requiring intubation
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during the trial up to 1 year from study start
Awards & highlights

CEASEVAP Trial Summary

This trial tests a new medical device that might reduce the risk of ventilator-associated pneumonia (VAP), which can result in increased duration of mechanical ventilation, increased ICU/hospital stay, increased risk of death and increased health care costs.

Who is the study for?
This trial is for adult critically ill patients with respiratory failure who need intubation but don't already have a tracheostomy or non-study endotracheal tube (ETT) when admitted to the ICU. Patients must consent to participate in research.Check my eligibility
What is being tested?
The study tests a new ETT coated with an antibiotic compound, CeraShield, against standard tubes with secretion drainage. It aims to see if this can prevent ventilator-associated pneumonia by reducing bio-film and bacteria on the ETT.See study design
What are the potential side effects?
Potential side effects are not explicitly listed, but may include reactions to the antibiotic coating such as local irritation or allergic responses. The usual risks of using any ETT also apply.

CEASEVAP Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am an adult in critical condition needing a breathing tube for respiratory failure.

CEASEVAP Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during the trial up to 1 year from study start
This trial's timeline: 3 weeks for screening, Varies for treatment, and during the trial up to 1 year from study start for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Occurrence of Ventilator Associated Pneumonia
Secondary outcome measures
Acceptability of the Intervention
Airway outcomes
Antibiotic Utilization
+5 more

CEASEVAP Trial Design

2Treatment groups
Active Control
Group I: Endotracheal Tube with Subglottic Secretion DrainageActive Control1 Intervention
All patients in this arm will be intubated with an ETT with subglottic secretion drainage
Group II: CeraShield Endotracheal TubeActive Control1 Intervention
All patients in this arm will be intubated with a ceragenin coated ETT

Find a Location

Who is running the clinical trial?

Queen's UniversityLead Sponsor
365 Previous Clinical Trials
120,017 Total Patients Enrolled
Dr. John MuscedereLead Sponsor
3 Previous Clinical Trials
790 Total Patients Enrolled
John MUSCEDERE, MDPrincipal InvestigatorQueens University

Media Library

CeraShield Endotracheal Tube (Antibiotic Compound Coating) Clinical Trial Eligibility Overview. Trial Name: NCT05761613 — N/A
Bacterial Pneumonia Research Study Groups: Endotracheal Tube with Subglottic Secretion Drainage, CeraShield Endotracheal Tube
Bacterial Pneumonia Clinical Trial 2023: CeraShield Endotracheal Tube Highlights & Side Effects. Trial Name: NCT05761613 — N/A
CeraShield Endotracheal Tube (Antibiotic Compound Coating) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05761613 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any current opportunities for individuals to enroll in this research?

"Data on clinicaltrials.gov shows that this trial is actively seeking patient participants, with the first post being made on February 21st 2023 and an update to it occurring six days later."

Answered by AI

How many volunteers are being enrolled in this clinical trial?

"That is accurate. As per clinicaltrials.gov, this research study commenced on February 21st 2023 and has been amended as recently as February 27th 2023. The trial seeks to enrol 400 participants from 1 distinct medical centre."

Answered by AI
~185 spots leftby Apr 2025