[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100602967":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":27,"locations":11,"responsibleParty":32,"collaborators":11,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":39,"acronym":11,"eligibilityCriteria":40,"healthyVolunteers":41,"sex":42,"minAge":43,"maxAge":11,"enrollmentInfo":44,"targetDuration":11,"studyType":47,"phases":48,"briefSummary":50,"conditions":51,"keywords":11,"overallStatus":54,"whyStopped":11,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":11},{"fullName":5,"class":6},"Metagenics, Inc.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"PhytoMulti® Multivitamin and UltraFlora® Balance Probiotic arm","ACTIVE_COMPARATOR",null,[13],"Dietary Supplement: Multivitamin and a Probiotic",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":11},"DIETARY_SUPPLEMENT","Multivitamin and a Probiotic","The duration of trial intervention and participation for an individual participant is approximately 3 months (12 weeks). Screening, during which eligibility to participate in the trial is assessed, occurs at baseline. A fixed, orally administered, dose of the study products (PhytoMulti® Multivitamin, 2 tablets\u002Fday and UltraFlora® Balance Probiotic, 1 capsule\u002Fday) are taken daily with breakfast",[9],[21,24],{"name":22,"affiliation":5,"role":23},"Mieke Van Den Driessche, PhD","STUDY_DIRECTOR",{"name":25,"affiliation":5,"role":26},"Irfan Qureshi, MD","PRINCIPAL_INVESTIGATOR",[28],{"name":25,"role":29,"phone":30,"phoneExt":11,"email":31},"CONTACT","+1 800-843-9660","trials@metagenics.com",{"type":33,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100602967","impact-of-multivitamin-phytomulti-and-a-probiotic-ultraflora-balance-probiotic-on-gut-health-of-people-taking-glp-1-medication-100602967",false,"NCT07130396","Impact of Multivitamin (PhytoMulti®) and a Probiotic (UltraFlora® Balance Probiotic) on Gut Health of People Taking GLP-1 Medication","A Single Arm Trial to Evaluate the Effect of PhytoMulti® Multivitamin and UltraFlora® Balance Probiotic on Bowel Symptoms in Individuals Using GLP-1 Receptor Agonists, Assessed by the IBS Symptom Severity Score (IBS-SSS)","Inclusion Criteria:\n\n1. Providing written informed consent\n2. Males and females of at least 18 years old\n3. Minimum 4 weeks on GLP-1 (f.e Ozempic®, Wegovy®, Mounjaro®, etc.) and maximum 1 year on GLP-1\n4. Body Mass Index (BMI) ≥ 25 AND ≤ 30\n5. Being willing to maintain stable dietary habits and physical activity levels throughout the trial period\n6. Being willing not to introduce any other food supplements during the trial period (supplements used in the two weeks prior to enrolling in the trial and used consistently throughout are acceptable, except for probiotics).\n\nExclusion Criteria:\n\n1. Having had any type of bariatric surgery, or planned bariatric surgery during the period of trial participation.\n2. Suffering from a severe chronic disease (e.g., cancer, HIV, hepatic or renal impairment, diabetes type I), inflammatory bowel disease (IBD), Coeliac Disease, and\u002For being immunocompromised.\n3. Suffering from any uncontrolled endocrine disorder\n4. Having used any antibiotic treatment in the 2 months prior to enrollment.\n5. Having a known allergy to the ingredients in the study product.\n6. Being pregnant or lactating (breastfeeding) or trying to become pregnant.\n7. Participating in another clinical trial.\n8. Suffering from dementia or inability to take the trial treatment in an appropriate way.\n9. Taking PhytoMulti® Multivitamin and\u002For UltraFlora® Probiotic or any similar product from competitors prior to trial participation",true,"ALL","18 Years",{"count":45,"type":46},100,"ESTIMATED","INTERVENTIONAL",[49],"NA","This is a single-arm, open-label clinical trial involving 100 participants who will undergo a total participation period of 12 weeks.",[52,53],"GLP-1","Adults","NOT_YET_RECRUITING","2025-08-12",{"date":57,"type":58},"2025-08-19","ACTUAL",{"date":60,"type":46},"2025-11-01",{"date":62,"type":46},"2026-04-30",{"name":5,"class":6}]