Pharmacokinetics of Voriconazole in Adult ECMO Patients
Launched by UNIVERSITY HOSPITALS, LEICESTER · Apr 27, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how the medication voriconazole works in adult patients who are on ECMO, a form of life support used in serious cases. Voriconazole is an antifungal medication that can help treat infections caused by fungi, particularly in patients who are critically ill with conditions like influenza, COVID-19, or serious fungal infections. The goal of the study is to determine the best dose of voriconazole for these patients, ensuring it is both effective and safe.
To participate in this study, individuals must be adults aged 18 and older who are currently in the ICU and receiving ECMO support. They also need to have tested positive for influenza or COVID-19 and have signs of a fungal infection. Participants will be monitored closely during the trial to understand how their bodies process the medication. This research is important because it aims to improve treatment for patients facing severe respiratory infections complicated by fungal infections, ultimately helping them recover better.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Adults aged ≥18 years
- • 2. Admitted to ICU on ECMO support
- • 3. Positive influenza or SARS-CoV-2 PCR from nasal, throat swab, BAL or other respiratory specimen.
- • 4. Positive invasive aspergillosis infection (positive Aspergillus species culture from respiratory specimen or positive serum galactomannan) or strong clinical suspicion of invasive aspergillosis infection based on symptoms, CT, CXR.
- Exclusion Criteria:
- • 1. No participants \< 18 years of age
- • 2. Not requiring ECMO support
- • 3. No positive influenza or SARS-CoV-2 results
- • 4. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
About University Hospitals, Leicester
University Hospitals Leicester (UHL) is a leading healthcare provider and clinical trial sponsor dedicated to advancing medical research and improving patient care through innovative clinical studies. As a prominent academic institution, UHL combines cutting-edge clinical practice with rigorous scientific inquiry, facilitating a collaborative environment for researchers, healthcare professionals, and patients. The organization is committed to conducting high-quality, ethically responsible trials across various therapeutic areas, striving to translate research findings into tangible health benefits for the diverse communities it serves. With a strong emphasis on patient safety and effective outcomes, UHL plays a vital role in shaping the future of healthcare through its dedication to clinical excellence and research advancement.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Leicester, , United Kingdom
Patients applied
Trial Officials
Hakeem Yusuff, MD
Principal Investigator
University Hospitals, Leicester
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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