Oral Care With 3% Hydrogen Peroxide (Oroxid®) in ICU - Effects on the Lower Airway Microbial Colonisation
Launched by CHARLES UNIVERSITY, CZECH REPUBLIC · Sep 19, 2023
Trial Information
Current as of November 08, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial, called HyPerMICROBE, is investigating the effects of daily oral care using a 3% hydrogen peroxide solution (Oroxid®) compared to standard care (0.2% chlorhexidine) for patients in the Intensive Care Unit (ICU) who are on mechanical ventilation. The goal is to see if using hydrogen peroxide can help reduce the growth of harmful bacteria in the lungs, which can lead to a serious condition known as ventilator-associated pneumonia (VAP).
To participate in this trial, individuals must be at least 18 years old, expected to stay in the ICU for more than five days, and need mechanical ventilation for at least 72 hours. Participants will be closely monitored, and those who qualify will receive either the hydrogen peroxide treatment or the standard care as part of their daily oral hygiene routine. This trial aims to find out if the new treatment is more effective in preventing infections compared to the usual method. It's important to note that some patients may not be eligible, especially those with certain medical conditions or who are pregnant.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥18 years
- • 2. In-patient of ICU and expected to stay \> 5 days
- • 3. Mechanical ventilation or imminent need of it; predicted length of mechanical ventilation (MV) ≥ 72h
- • 4. Clinical Pulmonary Infection score (CPIS) less than 6 at the baseline
- • 5. No history and symptoms of aspiration at the baseline
- Exclusion Criteria:
- • 1. ATB therapy of respiratory infection on admission
- • 2. Suspected pulmonary infection on admission and in the first 48h of mechanical ventilation
- • 3. Pregnancy
- • 4. Oral ulcers or injuries
- • 5. Patient with a history of hydrogen peroxide allergy
About Charles University, Czech Republic
Charles University, located in the Czech Republic, is a prestigious institution renowned for its commitment to advancing medical research and education. As a clinical trial sponsor, the university leverages its extensive academic expertise and state-of-the-art facilities to conduct innovative research that aims to improve patient outcomes and contribute to the global medical community. With a focus on ethical standards and rigorous scientific methodologies, Charles University collaborates with various stakeholders to explore new therapies and enhance healthcare practices, fostering a culture of excellence in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Praha, Czechia
Patients applied
Trial Officials
Kateřina Jiroutková, MD
Principal Investigator
3rd Faculty of Medicine, Charles University and FNKV, Prague
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported