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CeraShield Endotracheal Tube for Ventilator-Associated Pneumonia (CEASEVAP Trial)
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.
CEASEVAP Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowCEASEVAP Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.CEASEVAP Trial Design
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Who is running the clinical trial?
Media Library
- I am an adult in critical condition needing a breathing tube for respiratory failure.I had a tracheostomy when I was admitted to the ICU.You are currently in the hospital or ICU with a breathing tube that is not part of this study.I cannot be intubated with a standard endotracheal tube.
- Group 1: Endotracheal Tube with Subglottic Secretion Drainage
- Group 2: CeraShield Endotracheal Tube
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
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."
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."
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