A Pilot Study of Oral Tinidazole for Women With Recurrent Bacterial Vaginosis
Recurrent Bacterial Vaginosis
About this trial
This is an interventional treatment trial for Recurrent Bacterial Vaginosis focused on measuring Bacterial vaginosis, Tinidazole, Vaginitis
Eligibility Criteria
Inclusion Criteria: Current infection with bacterial vaginosis 2 previous episodes of bacterial vaginosis within the past 12 months Willing to use contraception Able to swallow pills Willing to refrain from douching or using vaginal products Willing to refrain from alcohol consumption 24 hours before and for 72 hours after taking study medication (tinidazole) Exclusion Criteria: Women with same sex partners Menstruating at initial exam Presence of yeast, a sexually transmitted disease, or other vaginal infection Purulent cervical discharge Use of any drug for bacterial vaginosis or yeast within the past 2 weeks prior to enrollment Pregnant or nursing Taking lithium Taking blood thinners (anticoagulation therapy) Use of any investigational drug within the previous 30 days Active HPV infection requiring treatment Use of drugs that suppress the immune system History of alcoholism Taking disulfiram
Sites / Locations
- Kaiser Permanente