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Treatment of Bacterial Vaginosis With Oral Tinidazole

Primary Purpose

Bacterial Vaginosis

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Tinidazole
Sponsored by
Mission Pharmacal
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bacterial Vaginosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Clinical and microbiological diagnosis of bacterial vaginosis - Exclusion Criteria: Other sexually transmitted disease -

Sites / Locations

  • Duke University School of Medicine

Outcomes

Primary Outcome Measures

Therapeutic efficacy
Safety

Secondary Outcome Measures

Clinical efficacy
Microbiological efficacy

Full Information

First Posted
September 27, 2005
Last Updated
March 21, 2017
Sponsor
Mission Pharmacal
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1. Study Identification

Unique Protocol Identification Number
NCT00229216
Brief Title
Treatment of Bacterial Vaginosis With Oral Tinidazole
Official Title
A Phase III Randomized, Multi-center, Double-blind, Double-dummy, Placebo-controlled Treatment Trial of Bacterial Vaginosis With Tinidazole Oral Tablets.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
June 2007 (Actual)
Study Completion Date
June 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Mission Pharmacal

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to confirm the safety and efficacy of oral tinidazole for the treatment of bacterial vaginosis.
Detailed Description
Tinidazole is a second-generation nitroimidazole i.e. an updated form of the standard drug used to treat bacterial vaginosis (metronidazole). Two dosing regimens are being compared to placebo to treat bacterial vaginosis, one of the most common vaginal infections.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Vaginosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Tinidazole
Primary Outcome Measure Information:
Title
Therapeutic efficacy
Title
Safety
Secondary Outcome Measure Information:
Title
Clinical efficacy
Title
Microbiological efficacy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical and microbiological diagnosis of bacterial vaginosis - Exclusion Criteria: Other sexually transmitted disease -
Facility Information:
Facility Name
Duke University School of Medicine
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17666604
Citation
Livengood CH 3rd, Ferris DG, Wiesenfeld HC, Hillier SL, Soper DE, Nyirjesy P, Marrazzo J, Chatwani A, Fine P, Sobel J, Taylor SN, Wood L, Kanalas JJ. Effectiveness of two tinidazole regimens in treatment of bacterial vaginosis: a randomized controlled trial. Obstet Gynecol. 2007 Aug;110(2 Pt 1):302-9. doi: 10.1097/01.AOG.0000275282.60506.3d.
Results Reference
derived

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Treatment of Bacterial Vaginosis With Oral Tinidazole

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