跳至主要内容
临床试验/NCT01055106
NCT01055106已完成2 期

A Multicenter, Randomized, Investigator-Blinded, Phase 2, Dose Ranging Study of Metronidazole Vaginal Gel in the Treatment of Bacterial Vaginosis

Graceway Pharmaceuticals, LLC20 个研究点 分布在 1 个国家目标入组 255 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
255
试验地点
20
主要终点
proportion of subjects with therapeutic cure

研究概览

简要总结

The objective of this study is to evaluate the efficacy and safety of GW05 administered in 3 regimens versus metronidazole 0.75% for the treatment of bacterial vaginosis.

详细描述

This is a multicenter, randomized, investigator-blinded, phase 2, dose ranging study of GW05 vaginal gel administered in 3 regimens compared to metronidazole 0.75% (QD x 5 days) for the treatment of bacterial vaginosis. Subjects will be evaluated at three timepoints (1 screening/baseline visit, post-treatment phone call and 1 test-of-cure visit). The total study duration may be up to 30 days for a subject.

Study medication will be applied intravaginally once daily at bedtime according to the assigned dosing schedule using the supplied 5-gram vaginal applicators.

Investigator blinding will be ensured by utilizing an independent drug dispensing coordinator at each site.

Bacterial vaginosis (BV) is an infection of the vagina (birth canal) that is the result of an overgrowth of bacteria that are often normally found in the vagina. This type of vaginal infection typically does not cause irritation. The most common complaint of patients who suffer from BV is a fishy-smelling vaginal discharge. The amount of vaginal discharge may or may not be increased above a normal discharge. The bad odor may get worse after sexual intercourse or during the menstrual period. BV is also strongly associated with problems during pregnancy, such as premature (early) birth, and with an increased risk of sexually transmitted diseases. Therefore, it is important to treat the infection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Females at least 18 years of age
  • In good general health
  • Confirmed current diagnosis of bacterial vaginosis (determined at study screening)
  • Negative pregnancy test (for women who are able to become pregnant)
  • Must abstain from sexual intercourse throughout the first 7 days of thes study
  • Must abstain from alcohol ingestion during the treatment period and for one day afterward
  • Must not use intra-vaginal products for the duration of the study

排除标准

  • Pregnant, lactating, or planning to become pregnant during the study period
  • Menstruating at the time of the diagnosis or anticipate the onset of menses during the treatment phase of the study
  • Had a medical event within 90 days of the visit (e.g., stroke, heart attack, etc.)
  • Received specific treatments/medications /therapy within the designated time period prior to study enrollment

研究组 & 干预措施

1D

Active Comparator

干预措施: GW05 (Drug)

3D

Active Comparator

干预措施: GW05 (Drug)

5D

Active Comparator

干预措施: GW05 (Drug)

Metronidazole

Active Comparator

干预措施: Metronidazole (Drug)

结局指标

主要结局

proportion of subjects with therapeutic cure

时间窗: day 21 to day 30

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (20)

Loading locations...

相似试验