Helfgott Research Institute National University of Natural Medicine
Portland, Oregon, 97201, United States
NCT Number: NCT03735420
A pilot study to assess the safety and tolerability of oral xanthohumol in humans, to identify a biological signature of xanthohumol exposure, and to characterize the role of xanthohumol metabolism by intestinal microorganisms in that signature.
This study is active but is not currently recruiting participants.
21 year–50 year
All sexes
Interventional
Phase 1
Portland, Oregon, 97201, United States
This is a double-masked, placebo controlled, randomized clinical trial of xanthohumol, which is a constituent of hops (Humulus lupulus). Hops and its constituents have a long history of use for a variety of conditions. However, knowledge is limited regarding the measurable biological markers of human exposure, and the role of xanthohumol metabolism by microorganisms present in the gut. This information is necessary for the development of xanthohumol as a potential therapeutic intervention in conditions such as inflammatory bowel disease.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The xanthohumol supplement will be administered in a capsule. Participants in the experimental arm will consume the capsule once per day, with the first meal. The intervention will extend for 8 weeks.
The placebo (vehicle) will be administered in a capsule. Participants in the placebo arm will consume the capsule once per day, with the first meal.
Other names: Vehicle
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Circulating pro-inflammatory cytokine concentrations (tumor necrosis factor (TNF)-α, interleukin (IL)-1 beta, IL-6, IL-8, IL-10, and IL-12p70), will be measured simultaneously with a flow cytometry-based multiplex assay. The measures were assessed at Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks; weeks 2, 4, 6, and 8 reported
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Self-reported adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events. Reported as: New onset "FDA serious" adverse events (Grade 1); New onset "moderate" adverse events (Grade 2). The measures were assessed at Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks; weeks 2, 4, 6, and 8 reported.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Xanthohumol and xanthohumol metabolites in blood, urine and stool, will be measured by ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry. Metabolites include 6-prenylnaringenin (6-PN), 8-prenylnaringenin (8-PN), dihydroxanthohumol (DXN), desmethyldihydroxanthohumol (DDXN), isoxanthohumol (IXN), and xanthohumol (XN). The measures were assessed at Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks; baseline, weeks 2, 4, 6, and 8 reported for urine and plasma.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Xanthohumol and xanthohumol metabolites in blood, urine and stool, will be measured by ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry. Metabolites include 6-prenylnaringenin (6-PN), 8-prenylnaringenin (8-PN), dihydroxanthohumol (DXN), desmethyldihydroxanthohumol (DDXN), isoxanthohumol (IXN), and xanthohumol (XN). The measures were assessed at Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks; baseline, weeks 2, 4, 6, and 8 reported for urine and plasma. As stool metabolites have not yet been analyzed, data will be released upon assessment.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Bile acid concentrations in blood and feces, will be measured by ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry, and expressed as mean change over time from baseline.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Fecal calprotectin, a protein associated with gut inflammation and irritable gut syndrome, will be measured by enzyme-linked immunosorbent assay, and expressed as mean change over time from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Aspartate aminotransferase is an enzyme that is often measured in blood as an indication of liver toxicity. Reported as mean change from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Alanine aminotransferase is an enzyme that is often measured in blood as an indication of liver toxicity. Reported as mean change from baseline.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks
Gamma-glutamyl transferase is an enzyme that is often measured in blood as an indication of liver toxicity. Reported as mean change from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks
Glomerular filtration rate is estimated based on blood creatinine concentration per standard nephrology practice. Reported as mean change from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Blood urea nitrogen (BUN) : creatinine (Cr) is a ratio of serum concentrations of two compounds associated with renal function. Reported as mean change from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of the various subtypes of blood cells (i.e., red blood cells, white blood cells, and platelets), plus indices including mean corpuscular hemoglobin (MCH), mean corpuscular volume (MCV), and hematocrit. Reported as: % abnormal (i.e., number of participants with an abnormal value compared to the number of participants in the group) and % new abnormals if abnormal counts were noted. Abnormality is assessed according to standards for age and sex measurements under Quest Diagnostics criteria.
Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of total red blood cell count. Reported as mean change from baseline.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of total white blood cell count. Results are reported as mean change from baseline at weeks 2, 4, 6, and 8.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of platelet count. Results are reported as mean change from baseline at weeks 2, 4, 6, and 8.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of mean corpuscular volume (MCV). Results are reported as mean change from baseline at weeks 2, 4, 6, and 8.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of mean corpuscular hemoglobin (MCH). Results are reported as mean change from baseline at weeks 2, 4, 6, and 8.
Time frame: 2 weeks, 4 weeks, 6 weeks, and 8 weeks.
Enumeration of hematocrit. Results are reported as mean change from baseline at weeks 2, 4, 6, and 8.
National University of Natural Medicine
Other
Xanthohumol Metabolism and Signature (XMaS) in Healthy Adults
Acronym: XMaS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07482644
Healthy, Inflammation
Pleasant Grove, Utah, United States
View Trial DetailsNCT07715864
Brain Concussion, Brain Diseases
Regina, Saskatchewan, Canada
View Trial DetailsNCT06527248
Cardiovascular Diseases, Healthy
Vienna, State of Vienna, Austria
View Trial DetailsNCT07008586
Behavior, Healthy
Cambridge, United Kingdom
View Trial Details