Xanthohumol as an Adjuvant Therapy in Critically Ill COVID-19 Patients
COVID-19 Respiratory Infection
About this trial
This is an interventional treatment trial for COVID-19 Respiratory Infection
Eligibility Criteria
Inclusion Criteria:
Adult patients aged 18 years or older, who are admitted to the ICU due to severe COVID-19-related acute respiratory failure (PaO2/FiO2 below 150).
Exclusion Criteria:
Patients who are treated for COVID-19 for more than a week and with additional complications such as bacterial infection.
History of severe chronic cardiovascular, liver or/and kidney diseases. Patients, who required prolonged oxygen supplementation or domestic mechanical ventilation.
Pregnant women, Neoplastic diseases, Immunologic diseases Patients, who received immunomodulatory treatment.
Sites / Locations
- Medical University of Lublin
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Group Xn
Group C
Patients who received extract from Humulus lupus L rich in Xanthohumol (Hop-RXn™, BioActive-Tech Ltd, Lublin, Poland; http://xanthohumol.com.pl/) as an adjuvant therapy. Based on pharmacokinetics and bioactivity, Xn was administered enterally three times a day every 8 hours at a dose of 1.5 mg/kg body weight (4.5 mg/kg body weight/day) for 7 days. The first dose of Xn was administered within 4 hours after admission to the ICU.
Patients who received 0.9% NaCl at the oral volume 1 mL (similar to Xn volume) three times a day every 8 hours. The first dose of Xn was administered within 4 hours after admission to the ICU.