[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100579245":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":26,"responsibleParty":30,"collaborators":26,"id":32,"slug":33,"hasResults":34,"nctId":35,"briefTitle":36,"officialTitle":37,"acronym":26,"eligibilityCriteria":38,"healthyVolunteers":39,"sex":40,"minAge":41,"maxAge":42,"enrollmentInfo":43,"targetDuration":26,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":26,"overallStatus":52,"whyStopped":26,"lastUpdateSubmitDate":53,"lastUpdatePostDateStruct":54,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":26},{"fullName":5,"class":6},"Wecare Probiotics Co., Ltd.","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Probiotic group","EXPERIMENTAL","Conventional medication (ornidazole vaginal suppositories for 7 days) + 30B CFU\u002Fstrip\u002Fday LRa05 (before meals);",[13],"Dietary Supplement: Probiotic",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo group","PLACEBO_COMPARATOR","Conventional medication (ornidazole vaginal suppositories for 7 days) + maltodextrin, one strip\u002Fday (before meals);",[19],"Dietary Supplement: Placebo",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DIETARY_SUPPLEMENT","Probiotic","The experimental phase of this study will last 8 weeks and each subject will receive 4 follow-up visits (week 0, week 4, week 8, week 20).",[9],null,{"type":22,"name":28,"description":24,"armGroupLabels":29,"otherNames":26},"Placebo",[15],{"type":31,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100579245","effects-of-lacticaseibacillus-rhamnosus-lra05-on-bacterial-vaginosis-and-ovarian-function-in-women-100579245",false,"NCT06821789","Effects of Lacticaseibacillus Rhamnosus LRa05 on Bacterial Vaginosis and Ovarian Function in Women","Effects of Lacticaseibacillus Rhamnosus LRa05 on Bacterial Vaginosis and Ovarian Function in Women: a Randomized, Double-blind, Placebo-controlled Trial","Inclusion Criteria:\n\n1. 18 to 65 years old, sexual activity, premenopausal women;\n2. Nugent score for diagnosing BV ≥7;\n3. Signed informed consent.\n\nExclusion Criteria:\n\n1. Mixed vaginitis, such as vulvovaginal candidiasis (VVC), Trichomonas vaginalis (TV) infection, Chlamydia trachomatis (CT) infection or gonococcal vaginitis;\n2. history of systemic organic disease or psychiatric illness;\n3. Planning pregnancy, breastfeeding, menstruation;\n4. within 5 days of the onset of the disease, any antibiotics have been used;\n5. long-term use of contraceptives or immunosuppressants;\n6. Allergic constitution or hypersensitivity to known components of the study drug.",true,"FEMALE","18 Years","65 Years",{"count":44,"type":45},60,"ESTIMATED","INTERVENTIONAL",[48],"NA","In this study, Lacticaseibacillus rhamnosus LRa05 was selected as test preparations to observe the clinical efficacy in the intervention trial of combined antibiotic therapy, and to evaluate its effects on the cure rate, recurrence rate and vaginal microbiota of patients with bacterial vaginitis.",[51],"Patients With Bacterial Vaginosis","NOT_YET_RECRUITING","2025-02-14",{"date":55,"type":56},"2025-02-19","ACTUAL",{"date":58,"type":45},"2025-03-15",{"date":60,"type":45},"2026-05-30",{"name":5,"class":6}]