Using Xanthohumol to help treat septic shock
Official title: Analysis of Anti-inflammatory Effect of Hop Extract Rich in Xanthohumol in Patients Treated for Septic Shock
Run by Medical University of Lublin · NCT06225258 · Data updated 2026-11-12
This study is testing if a natural compound called Xanthohumol can help improve recovery for patients with septic shock who need breathing support.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Medical University of Lublin Academic / other |
| Locations | 1 site (Lublin, Lublin Voivodeship) |
| Status | Recruiting |
| Started | January 9, 2023 |
| Main results expected | October 30, 2025 |
| Study ends | December 31, 2025 |
| Registry record updated | July 4, 2025 |
| Trial ID | NCT06225258 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults in the early phase of septic shock with respiratory insufficiency requiring mechanical ventilation and specific inflammatory markers.
✕Probably not a fit
Patients with a history of severe chronic cardiac, pulmonary, or liver diseases may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the use of Xanthohumol as an adjuvant treatment for patients experiencing septic shock, a severe condition characterized by an overwhelming inflammatory response to infections. The study focuses on patients in the early acute phase of septic shock who require mechanical ventilation due to respiratory insufficiency. By targeting the inflammatory response and cytokine release associated with septic shock, the trial aims to improve organ function and patient outcomes. Participants will be closely monitored in an intensive care unit setting to assess the effectiveness of the intervention.
Why it matters
Potential benefit: If successful, this treatment could significantly improve recovery rates and organ function in patients suffering from septic shock.
How similar studies have gone: Previous studies have shown promise in reducing inflammatory responses in septic shock, suggesting that this approach may be beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * a septic shock in the early, acute phase, * respiratory insufficiency required mechanical ventilation with PaO2/FiO2 \< 150, * bacterial infection, * procalcitonin higher than 5 ng/mL and interleukin 6 higher than 100 pg/mL, * no allergy to hops or their derivatives, * hemodynamic instability requiring vasopressor infusions Exclusion Criteria: * lack of agreement * septic shock treated for more than 1 day, * history of severe chronic cardiac, pulmonary and/or liver diseases
Where it's running
-
Intensive Care Unit, University Hospital No 4,
Lublin, Lublin Voivodeship, Poland Recruiting
Study contacts
- Principal investigator: Wlodzimierz Plotek — Medical University of Lublin, Poland
- Study coordinator: Wojciech Dabrowski, Prof
- Email: wojciech.dabrowski@umlub.pl
- Phone: +48604241040
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.