[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100610005":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":29,"centralContacts":35,"locations":41,"responsibleParty":57,"collaborators":29,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":63,"acronym":29,"eligibilityCriteria":64,"healthyVolunteers":65,"sex":66,"minAge":67,"maxAge":68,"enrollmentInfo":69,"targetDuration":29,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":29,"overallStatus":79,"whyStopped":29,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Qualia Life Sciences","INDUSTRY",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Qualia Glutathione+ version 1","ACTIVE_COMPARATOR","Qualia Glutathione+ version 1 manufactured by Qualia Life Sciences",[13],"Dietary Supplement: Qualia Glutathione+ version 1",{"label":15,"type":10,"description":16,"interventionNames":17},"Qualia Glutathione+ version 2","Qualia Glutathione+ version 2 manufactured by Qualia Life Sciences",[18],"Dietary Supplement: Qualia Glutathione+ version 2",{"label":20,"type":21,"description":22,"interventionNames":23},"Placebo","PLACEBO_COMPARATOR","Rice flour placebo",[24],"Dietary Supplement: Placebo",[26,30,32],{"type":27,"name":9,"description":11,"armGroupLabels":28,"otherNames":29},"DIETARY_SUPPLEMENT",[9],null,{"type":27,"name":15,"description":16,"armGroupLabels":31,"otherNames":29},[15],{"type":27,"name":20,"description":33,"armGroupLabels":34,"otherNames":29},"Rice flour",[20],[36],{"name":37,"role":38,"phone":39,"phoneExt":29,"email":40},"William Scuba","CONTACT","855-281-2328","support@qualialife.com",[42],{"facility":5,"status":29,"city":43,"state":44,"zip":45,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Carlsbad","California","92011","United States","US",{"type":49,"coordinates":50},"Point",[51,52],-117.35059,33.15809,{"lat":52,"lon":51},[55],{"name":56,"role":38,"phone":39,"phoneExt":29,"email":40},"Study Coordinator",{"type":58,"investigatorFullName":29,"investigatorTitle":29,"investigatorAffiliation":29,"oldNameTitle":29,"oldOrganization":29},"SPONSOR","100610005","the-impact-of-qualia-gluthathione-on-blood-glutathione-levels-100610005",false,"NCT07221955","The Impact of Qualia Gluthathione+ on Blood Glutathione Levels","Inclusion criteria:\n\n* Provide voluntary, written, informed consent to participate in the study\n* Agree to provide a valid cell phone number and are willing to receive communications through text\n* Can read and write English\n* Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly\n* Willing to complete questionnaires, records, and diaries associated with the study.\n* Healthy male and female participants aged 45-75 years\n* Willing to go to a local blood draw location for a Whole Blood Total Glutathione measurement (baseline and Day 20)\n* Willing to avoid starting new or stopping any existing dietary supplements throughout the study\n\nExclusion criteria:\n\n* Women who are pregnant, breastfeeding, or planning to become pregnant during the trial\n* Known food intolerances\u002Fallergy to any ingredients in the product\n* Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, cancer\n* Having had a significant cardiovascular event in the past 6 months\n* Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines\n* On immunosuppressive therapy\n* Adults lacking capacity to consent\n* Active Smokers\n* Diagnosed Diabetics",true,"ALL","45 Years","75 Years",{"count":70,"type":71},54,"ESTIMATED","INTERVENTIONAL",[74],"NA","This is a randomized, double-blind, placebo-controlled, parallel-group, triple-armed, study evaluating the effects of two distinct Qualia Glutathione+ formulations on Whole Blood Glutathione levels in the blood of healthy adults aged 45-75 years. Approximately 18 participants will be randomized to one of three study arms: Qualia Glutathione+ version 1, Qualia Glutathione+ version 2, or placebo. Each participant will take two or three capsules of their assigned product once daily in the morning, with or without food, over a 20-day period. The primary outcome is the change in blood glutathione levels, assessed via in lab blood collection at baseline and study completion. Secondary endpoints include questionnaires measuring health-related quality of life, fatigue, and cognitive functioning (PROMIS Global Health-10, PROMIS Short Form v1.0 - Fatigue 10a, PROMIS Cognitive Function - Short Form 8a), evaluation of safety and tolerability, and an Overall Experience Questionnaire (Appendices 1, 4-7). All assessments, including electronic questionnaires, are completed remotely without in-person visits.",[77,78],"Effects of Qualia Glutathione+ on Blood Glutathione Levels","Glutathione","NOT_YET_RECRUITING","2025-11-12",{"date":82,"type":83},"2025-11-14","ACTUAL",{"date":85,"type":71},"2025-12-02",{"date":87,"type":71},"2026-01-25",{"name":5,"class":6},1]