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Xanthohumol as an Adjuvant Therapy in Critically Ill COVID-19 Patients

Primary Purpose

COVID-19 Respiratory Infection

Status
Suspended
Phase
Early Phase 1
Locations
Poland
Study Type
Interventional
Intervention
Xanthohumol - prenylated chalcone extracted from female inflorescences of hop cones (Humulus lupus). Hop-RXn™, BioActive-Tech Ltd, Lublin, Poland; http://xanthohumol.com.pl/
Sponsored by
Medical University of Lublin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 Respiratory Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Placebo Comparator

Arm Label

Group Xn

Group C

Arm Description

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.

Outcomes

Primary Outcome Measures

Xanthohumol reduces coronavirus-induced inflammatory response
Xanthohumol possesses strong anti-inflammatory properties. It can reduce the production and secretion of pro-inflammatory cytokines. Additionally, it inhibits inflammatory-induced endothelial dysregulation and exerting antiangiogenic and anti-inflammatory effects.
Xanthohumol improves clinical course in critically ill COVID-19 patients
Reduction the severity of inflammatory response should affect clinical course. Strong anti-inflammatory treatment can reduce a risk of poor outcome.

Secondary Outcome Measures

Full Information

First Posted
July 15, 2022
Last Updated
May 17, 2023
Sponsor
Medical University of Lublin
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1. Study Identification

Unique Protocol Identification Number
NCT05463393
Brief Title
Xanthohumol as an Adjuvant Therapy in Critically Ill COVID-19 Patients
Official Title
Humulus Lupus Extract Rich in Xanthohumol Improves Clinical Course in Critically Ill COVID-19 Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Suspended
Why Stopped
We are waiting for the additional founds.
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
January 30, 2022 (Actual)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Lublin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
It has been well documented that coronavirus COVID-19 disease is associated with massive inflammatory response and cytokine storm. Several medications have been used to ameliorate COVID-19-related inflammation. Xanthohumol, a natural medication extracted from hop cones, possesses strong anti-inflammatory properties and can reduce the severity of inflammatory response. The aim of this study is to analyze the effect of Xanthohumol on clinical course, inflammatory response and outcome in patients admitted to the ICU due to COVID-related acute respiratory failure with an oxygenation index (PaO2/FiO2) less than 150.
Detailed Description
Xanthohumol inhibits proinflammatory pathways in different independent mechanisms. Ir inhibits farnesoid X receptor activity, and reduces the synthesis and release of different proinflammatory cytokines such as IL-1β, IL-6, IL-8, IL-12p70, TNFα and interferon γ. The pathomechanism of its anti-inflammatory activity is associated with the suppression of nuclear factor-kappa B. Additionally, Xanthohumol inhibits inflammatory-induced endothelial disorders, which are associated with an improvement in blood velocity and a reduction in the risk of arterial thrombosis, especially in pulmonary arteries. An increase in proinflammatory release, known as cytokine storm, as well as increased incidences of vascular thrombosis, are observed in coronavirus infection. Hence, Xanthohumol may reduce the severity of the clinical course in COVID-19 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19 Respiratory Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Patients were randomized in a double-blind, placebo-controlled fashion into two groups using sealed envelopes
Masking
Investigator
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group Xn
Arm Type
Experimental
Arm Description
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.
Arm Title
Group C
Arm Type
Placebo Comparator
Arm Description
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.
Intervention Type
Biological
Intervention Name(s)
Xanthohumol - prenylated chalcone extracted from female inflorescences of hop cones (Humulus lupus). Hop-RXn™, BioActive-Tech Ltd, Lublin, Poland; http://xanthohumol.com.pl/
Intervention Description
The appropriate dose of Xanthohumol was solved in 1 mL of propylene glycol
Primary Outcome Measure Information:
Title
Xanthohumol reduces coronavirus-induced inflammatory response
Description
Xanthohumol possesses strong anti-inflammatory properties. It can reduce the production and secretion of pro-inflammatory cytokines. Additionally, it inhibits inflammatory-induced endothelial dysregulation and exerting antiangiogenic and anti-inflammatory effects.
Time Frame
one week after regular supplementation
Title
Xanthohumol improves clinical course in critically ill COVID-19 patients
Description
Reduction the severity of inflammatory response should affect clinical course. Strong anti-inflammatory treatment can reduce a risk of poor outcome.
Time Frame
28 days mortality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of COVID-19 with acute respiratory failure (PaO2/FiO2 below 150). Exclusion Criteria: History of chronic cardiovascular, liver or/and kidney diseases. History of chronic pulmonary diseases with prolonged oxygen supplementation or domestic mechanical ventilation. Pregnant women, Neoplastic diseases, Immunologic diseases Patients received immunomodulatory treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrzej Stepulak, Prof
Organizational Affiliation
Rector of the Medical University of Lublin, Poland
Official's Role
Study Director
Facility Information:
Facility Name
Medical University of Lublin
City
Lublin
ZIP/Postal Code
20-059
Country
Poland

12. IPD Sharing Statement

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Xanthohumol as an Adjuvant Therapy in Critically Ill COVID-19 Patients

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