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Vaginosis, Bacterial clinical trials

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NCT ID: NCT05788991 Terminated - Bacterial Vaginosis Clinical Trials

Comparison of Dequalinium Chloride (Fluomizin) vs Oral Metronidazole for the Treatment of Bacterial Vaginosis

Start date: July 26, 2021
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to show the efficacy and safety of dequalinium chloride in the treatment of bacterial vaginosis compared to metronidazole.

NCT ID: NCT04578015 Terminated - Bacterial Vaginoses Clinical Trials

A Randomized Controlled Trial of Treatment of Bacterial Vaginosis

Start date: April 26, 2021
Phase: Phase 4
Study type: Interventional

This is a double-blinded, placebo controlled, multi-center randomized trial of 482 pregnant women who are diagnosed with Bacterial Vaginosis (BV) in the late 3rd trimester (>34 weeks). During routine clinic visit after 34 weeks, prospective patients will be counseled about the study. Patients who agree to be enrolled, will sign informed consent. Following enrollment, patients will be screened for BV. Those patients who are BV positive by clinical diagnosis, will be randomized to receive either metronidazole 500 mg BID orally for 7 days or identically appearing placebo.

NCT ID: NCT03954990 Terminated - Bacterial Vaginoses Clinical Trials

Treatment of Bacterial Vaginosis Prior to Active Labor and Infectious Morbidity

Start date: October 11, 2019
Phase: Phase 1
Study type: Interventional

Bacterial vaginosis (BV) is the most common cause of vaginal discharge among repro-ductive aged women. It is been linked to adverse maternal and neonatal outcomes. Our objective is to evaluate if the use of a single dose of metronidazole in women with BV at time of delivery reduces infectious morbidities

NCT ID: NCT03943823 Terminated - Clinical trials for Vaginosis, Bacterial

Postmenopausal Pessary Users: Estrogen Versus Trimosan

Start date: May 7, 2019
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare vaginally applied estrogen with the vaginal gel trimosan for their effects on vaginal pH and vaginal symptoms in postmenopausal pessary users.

NCT ID: NCT02946346 Terminated - Bacterial Vaginosis Clinical Trials

Kinetics and Ecology of Human Papillomavirus Genital Infections in Young Women

PAPCLEAR
Start date: November 11, 2016
Phase: N/A
Study type: Interventional

Most genital infections by human papillomaviruses (HPV) are asymptomatic or benign and clear within a few months or years. There infections are much less studies than chronic infections, even though they represent the main reservoir for the virus. The goal of this project is to decipher the kinetics of the virus and of the host immune response in acute HPV genital infections in your women. This will be performed by following women longitudinally and regularly in order to measure variations in virus load, immune cell count, cytokine concentration and antibody titers. The investigators will also investigate the interaction between these kinetics and host genetics and host vaginal microbiota

NCT ID: NCT02376972 Terminated - BACTERIAL VAGINOSIS Clinical Trials

Efficacy and Safety Study of Rifaximin Vaginal Tablets in Bacterial Vaginosis

VARIANT
Start date: April 2015
Phase: Phase 2
Study type: Interventional

THE STUDY HAS BEEN DESIGNED TO COMPARE THE EFFICACY OF TWO DOSES (25 MG AND 100 MG) OF RIFAXIMIN VAGINAL TABLETS VERSUS PLACEBO IN SUBJECTS WITH BACTERIAL VAGINOSIS

NCT ID: NCT02197182 Terminated - Clinical trials for Bacterial Vaginosis (BV)

LUXSOL(TM) Topical Cream for the Treatment of Symptomatic Bacterial Vaginosis; A Proof of Concept Study

Start date: June 2014
Phase: Early Phase 1
Study type: Interventional

LUXSOL Cream may be useful for the treatment of bacterial Vaginosis. In this study, LUXSOL Cream is compared to a control arm group using metronidazole cream. LUXSOL is administered intravaginally for 10 days, each evening before bedtime to treat bacterial Vaginosis..

NCT ID: NCT01762670 Terminated - Bacterial Vaginosis Clinical Trials

GoldenCareTM for the Treatment of Bacterial Vaginosis

Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

GoldenCare is a copper intravaginal device that may be useful for the treatment of symptomatic bacterial Vaginosis (BV). Standard treatment for BV is metronidazole. Although the reported cure rate is as high as 90%, the recurrence rate is 58% after 12 months. The study hypothesis is that GoldenCare will cure BV. This is a proof of concept study to collect preliminary evidence of the safety and efficacy of GoldenCare.

NCT ID: NCT01322971 Terminated - Infertility Clinical Trials

Efficacy Study of Preconception Treatment of an Asymptomatic Bacterial Infection in an Infertility Population

Start date: February 2011
Phase: N/A
Study type: Interventional

Bacterial vaginosis (BV) is a common vaginal infection characterized by a pathologic shift in the normal vaginal flora. BV has been associated with a number of poor reproductive outcomes, including infertility, preterm labor and premature rupture of membranes. If BV does disrupt normal embryologic development, then the treatment of BV prior to conception may improve implantation rates and other pregnancy outcomes in the infertile population. This is a prospective, randomized, double-blind, placebo-controlled trial in which infertile women undergoing intrauterine insemination or embryo transfer are screened for BV prior to treatment. Those patients who screen positive for BV will then be randomized into the treatment arm(metronidazole 500mg by mouth twice daily for 7 days) or the control arm (placebo by mouth twice daily for 7 days). The primary outcome, positive pregnancy test rate (i.e. biochemical pregnancy rate), will then be assessed. Secondary outcomes, such as clinical pregnancy rate, miscarriage rate, and live birth rate will also be examined.

NCT ID: NCT01153958 Terminated - Clinical trials for Vaginosis, Bacterial

Colposeptine for the Treatment of Bacterial Vaginosis

Start date: July 2010
Phase: Phase 4
Study type: Interventional

This is a prospective, randomized, controlled and multi-center trial to assess the use of colposeptine in female subjects with bacterial vaginosis. A total of 480 subjects were planned to be enrolled in various centers in China.