[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100599177":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":19,"locations":25,"responsibleParty":41,"collaborators":11,"id":43,"slug":11,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":11,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":50,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":11,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":11,"overallStatus":28,"whyStopped":11,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Wecare Probiotics Co., Ltd.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Probiotic group","EXPERIMENTAL",null,[13],"Dietary Supplement: Probiotic group",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":11},"DIETARY_SUPPLEMENT","Participants took a freeze-dried probiotic powder every day, half an hour after a meal.",[9],[20],{"name":21,"role":22,"phone":23,"phoneExt":11,"email":24},"Ying Jin, Doctor","CONTACT","13375163966","sunny13211@sina.com",[26],{"facility":27,"status":28,"city":29,"state":30,"zip":31,"country":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"Suzhou Ninth People's Hospital Suzhou Ninth Hospital affiliated to Soochow University","RECRUITING","Suzhou","Jiangsu","215200","China",{"type":34,"coordinates":35},"Point",[36,37],120.59538,31.30408,{"lat":37,"lon":36},[40],{"name":21,"role":22,"phone":11,"phoneExt":11,"email":24},{"type":42,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100599177",false,"NCT07081100","Probiotics and Non-Organic Gastrointestinal Improvement","Study on the Effect of Probiotics on Improving Gastrointestinal Function in Patients With Non-organic Gastrointestinal Dysfunction","Inclusion Criteria:\n\n* Voluntarily sign the informed consent form and agree to participate in the study.\n* Ability to complete the study according to the trial protocol requirements.\n* Aged 18-65 years.\n* Clinical diagnosis of non-organic gastrointestinal dysfunction (e.g., functional dyspepsia, functional constipation) without other serious organic diseases.\n\nExclusion Criteria:\n\n* Use of drugs affecting intestinal flora (antibiotics, probiotics, intestinal mucosal protectants, herbal medicines, etc.) for \\>1 week within 1 month prior to screening.\n* Short-term use of products with functions similar to the investigational product, which may interfere with result interpretation.\n* Antibiotic use during the study period.\n* History of severe systemic diseases or malignancies.\n* Allergy to any ingredient in the compound probiotic freeze-dried powder used in the trial.\n* Pregnancy, lactation, or plans for pregnancy in the near future.\n* Inability to participate due to personal reasons.\n* Other conditions deemed unsuitable by the investigators.",true,"ALL","18 Years","65 Years",{"count":54,"type":55},50,"ESTIMATED","INTERVENTIONAL",[58],"NA","To verify the improvement of gastrointestinal function in patients with non-organic gastrointestinal dysfunction after 4 weeks of intervention with compound probiotics.",[61],"Gastrointestinal Function","2025-07-28",{"date":64,"type":65},"2025-07-31","ACTUAL",{"date":67,"type":55},"2025-08-05",{"date":69,"type":55},"2026-03-01",{"name":5,"class":6},1]