[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100577290":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":11,"centralContacts":34,"locations":40,"responsibleParty":55,"collaborators":11,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":65,"sex":66,"minAge":67,"maxAge":11,"enrollmentInfo":68,"targetDuration":11,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":11,"overallStatus":43,"whyStopped":11,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"University Medicine Greifswald","OTHER",[8,14,18,21],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm 2: Fisetin, fasted condition - Cohort 2: old age (≥ 65 years)","ACTIVE_COMPARATOR",null,[13],"Dietary Supplement: Fisetin - Fasted condition",{"label":15,"type":10,"description":11,"interventionNames":16},"Arm 4: Fisetin, fed condition - Cohort 2: old age (≥ 65 years)",[17],"Dietary Supplement: Fisetin - Fed condition",{"label":19,"type":10,"description":11,"interventionNames":20},"Arm 1: Fisetin, fasted condition - Cohort 1: young age (18-30 years)",[13],{"label":22,"type":10,"description":11,"interventionNames":23},"Arm 3: Fisetin, fed condition - Cohort 1: young age (18-30 years)",[17],[25,30],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":11},"DIETARY_SUPPLEMENT","Fisetin - Fasted condition","A single oral dose of 500 mg fisetin (as Novusetin®) will be administered as 5 capsules with 240 ml of still water in the overnight fasting condition:\n\nA total of 24 blood samples will be taken at defined time points (baseline; 10; 20; 30; 40; 50; 60; 80; 100 min; 2.0; 2.5; 3.0; 3.5; 4.0; 4.5; 5.0; 5.5; 6.0; 6.5; 7.0; 7.5; 8.0; 9.0; 10.0 h). At each time point, blood will be collected (4.9 ml for separation of plasma) to determine fisetin, and fisetin metabolites. The total amount of blood collected for each participant and each arm is 164 ml at the kinetic visits and 12 ml at the screening visit. Urine will be collected during the first 10 hours after fisetin administration.",[19,9],{"type":26,"name":31,"description":32,"armGroupLabels":33,"otherNames":11},"Fisetin - Fed condition","A single oral dose of 500 mg fisetin (as Novusetin®) will be administered as 5 capsules with 240 ml of still water in fed condition:\n\nParticipants will eat a high-caloric and high-fat meal based on the recommendation of the FDA (Food and Drug Administration) for food-effect studies. This meal will contain two slices of toast with butter, two eggs fried in butter, approx. 113 g hash brown potatoes and 240 ml whole milk.\n\nA total of 24 blood samples will be taken at defined time points (baseline; 10; 20; 30; 40; 50; 60; 80; 100 min; 2.0; 2.5; 3.0; 3.5; 4.0; 4.5; 5.0; 5.5; 6.0; 6.5; 7.0; 7.5; 8.0; 9.0; 10.0 h). At each time point, blood will be collected (4.9 ml for separation of plasma) to determine fisetin, and fisetin metabolites. The total amount of blood collected for each participant and each arm is 164 ml at the kinetic visits and 12 ml at the screening visit. Urine will be collected during the first 10 hours after fisetin administration.",[22,15],[35],{"name":36,"role":37,"phone":38,"phoneExt":11,"email":39},"Stefan Engeli, Prof.","CONTACT","+49 3834 86 56 33","stefan.engeli@med.uni-greifswald.de",[41],{"facility":42,"status":43,"city":44,"state":11,"zip":11,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Department of Clinical Pharmacology, Institute of Pharmacology at the Center of Drug Absorption and Transport (C_DAT), University Medicine Greifswald","RECRUITING","Greifswald","Germany","DE",{"type":48,"coordinates":49},"Point",[50,51],13.40244,54.08905,{"lat":51,"lon":50},[54],{"name":36,"role":37,"phone":38,"phoneExt":11,"email":39},{"type":56,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100577290","a-comparison-of-fisetin-kinetics-in-young-and-old-adults-100577290",false,"NCT06796374","A Comparison of Fisetin Kinetics in Young and Old Adults","A Comparison of Fisetin Kinetics in Young and Old Adults - FISEKIN-1","FISEKIN-1","Inclusion Criteria:\n\n* any sex\n* age between 18 and 30 years or ≥ 65 years\n* understands the study purpose and design\n* contractually capable and provides signed informed consent form\n* healthy condition or mild and\u002For well-treated forms of allergies, asthma, hypertension, and orthopedic diseases\n* a maximum of 3 chronically taken drugs\n\nExclusion Criteria:\n\n* BMI \\> 30 kg\u002Fm2 and \\\u003C 18 kg\u002Fm2\n* body weight \\\u003C 48 kg\n* women in young cohort: known pregnancy or lactation period; positive urine pregnancy test at screening or kinetic visit\n* men: hemoglobin \\\u003C 8,3 mmol\u002Fl women: hemoglobin \\\u003C 7,3 mmol\u002Fl\n* elevated liver function tests (1 or more of ALAT, ASAT, yGT, Bilirubin \\> 2x ULN)\n* reduced renal function (eGFRMDRD \\\u003C 60 ml\u002Fmin\u002F1,7 m2)\n* QTcF \\> 450 ms in screening ECG\n* psychiatric disease requiring recent or actual treatment\n* drug dependency at the time of visit\n* use of recreational drugs more than twice a week\n* any known hypersensitivity or allergic reactions to fisetin\n* history of severe hypersensitivity reactions and\u002For anaphylaxis\n* poor venous conditions that make it impossible to place a peripheral venous catheter and regularly draw blood through it\n* intake of drugs undergoing extensive metabolism via CYP1A2, CYP2D6, CYP2C8, CYP2C9, CYP2C19, CYP3A4, and\u002For Pgp and with narrow (monitoring-requiring) therapeutic range during the past seven days if the duration of intake was at least two days\n* intake of COMT-inhibitors during the past seven days if the duration of intake was at least two days\n* intake of drugs or dietary supplements containing fisetin within the two days before or during the kinetic visits\n* individuals who have eaten food with high fisetin content in the two days before the kinetic visits (e.g. strawberry, apple, persimmon, grape, mango, kiwi, peach, tomato, onion, lotus roots, kale, cucumber; processed products, e.g. wine)",true,"ALL","18 Years",{"count":69,"type":70},80,"ESTIMATED","INTERVENTIONAL",[73],"NA","This study investigates the differences in the kinetic parameters of fisetin in two cohorts of healthy volunteers:\n\nCohort 1) volunteers aged 18-30 years (n = 40) Cohort 2) volunteers aged 65 years or older (n = 40)\n\nThe purpose of this study is:\n\n1. To describe the fisetin kinetics after a single dose oral administration in older age.\n2. To compare the fisetin kinetics after a single dose oral administration in old and young age.\n\nFISEKIN-1 is designed as a four-arm study protocol. As well as two different age groups (18-30 years vs. 65 years and older), we want to compare fisetin kinetic parameters in fasted and fed condition:\n\nArm 1) 500 mg fisetin (1x 5 capsule), fasted condition, cohort 1: young age Arm 2) 500 mg fisetin (1x 5 capsule), fasted condition, cohort 2: old age Arm 3) 500 mg fisetin (1x 5 capsule), fed condition, cohort 1: young age Arm 4) 500 mg fisetin (1x 5 capsule), fed condition, cohort 2: old age",[76],"Pharmacokinetic Study in Healthy Volunteers","2026-03-31",{"date":79,"type":80},"2026-04-06","ACTUAL",{"date":77,"type":70},{"date":83,"type":70},"2027-07-31",{"name":5,"class":6},1]