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Dose Ranging Study of Metronidazole Vaginal Gel in the Treatment of Bacterial Vaginosis

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01055106
First Posted: January 25, 2010
Last Update Posted: July 1, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Graceway Pharmaceuticals, LLC
January 21, 2010
January 25, 2010
July 1, 2011
January 2010
April 2010   (Final data collection date for primary outcome measure)
proportion of subjects with therapeutic cure [ Time Frame: day 21 to day 30 ]
Same as current
Complete list of historical versions of study NCT01055106 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
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Dose Ranging Study of Metronidazole Vaginal Gel in the Treatment of Bacterial Vaginosis
A Multicenter, Randomized, Investigator-Blinded, Phase 2, Dose Ranging Study of Metronidazole Vaginal Gel in the Treatment of Bacterial Vaginosis
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.

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.

Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
  • Vaginosis, Bacterial
  • Vaginal Infection
  • Drug: GW05
    vaginal gel once daily regimen A
  • Drug: GW05
    vaginal gel once daily regimen B
  • Drug: GW05
    vaginal gel once daily regimen C
  • Drug: Metronidazole
    vaginal gel 0.75% once daily for 5 days
  • Active Comparator: 1D
    Intervention: Drug: GW05
  • Active Comparator: 3D
    Intervention: Drug: GW05
  • Active Comparator: 5D
    Intervention: Drug: GW05
  • Active Comparator: Metronidazole
    Intervention: Drug: Metronidazole
Chavoustie SE, Jacobs M, Reisman HA, Waldbaum AS, Levy SF, Hillier SL, Nyirjesy P. Metronidazole vaginal gel 1.3% in the treatment of bacterial vaginosis: a dose-ranging study. J Low Genit Tract Dis. 2015 Apr;19(2):129-34. doi: 10.1097/LGT.0000000000000062.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
255
April 2010
April 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
Sexes Eligible for Study: Female
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01055106
GW05-0904
No
Not Provided
Not Provided
Sharon F. Levy, MD / Vice President Product Develpoment, Graceway Pharmaceuticals
Graceway Pharmaceuticals, LLC
Not Provided
Study Director: Sharon F Levy, MD Graceway Pharmaceuticals
Graceway Pharmaceuticals, LLC
June 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP