ConditionPatients With Bacterial Vaginosis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorWecare Probiotics Co., Ltd.
About this trial
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.
Eligibility criteria
Qualifiers
18 to 65 years old, sexual activity, premenopausal women;
Nugent score for diagnosing BV ≥7;
Signed informed consent.
Disqualifiers
Mixed vaginitis, such as vulvovaginal candidiasis (VVC), Trichomonas vaginalis (TV) infection, Chlamydia trachomatis (CT) infection or gonococcal vaginitis;
history of systemic organic disease or psychiatric illness;
Planning pregnancy, breastfeeding, menstruation;
within 5 days of the onset of the disease, any antibiotics have been used;
Trial design
Treatments tested in this trial
- Probiotic
- Placebo
Treatment groups
60 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov