Safety and Efficacy Study to Treat Bacterial Vaginosis

Completed · Phase 3 · Has a placebo group

Conditions studied: Bacterial Vaginosis

In brief

The purpose of this study is to determine if product 55394 is safe and efficacious for the treatment of bacterial vaginosis.

Key facts

Study ID

NCT01621399

Run by

Medicis Global Service Corporation

People needed

651

Starts

2012-05-01

Expected to finish

2012-12-01

Last updated by the study team

2013-08-21

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Have a clinical diagnosis of bacterial vaginosis as determined by the investigator.
• Other items as identified in the protocol.

You may not qualify if…

• Have a known or suspected other infectious cause of vulvovaginitis.
• Other items as identified in the protocol.

Where it is running

• Study site — Birmingham, Alabama, United States
• Study site — Phoenix, Arizona, United States
• Study site — La Mesa, California, United States
• Study site — Los Angeles, California, United States
• Study site — San Diego, California, United States
• Study site — Torrance, California, United States
• Study site — Denver, Colorado, United States
• Study site — Groton, Connecticut, United States
• Study site — Boyton Beach, Florida, United States
• Study site — Clearwater, Florida, United States
• Study site — Miami, Florida, United States
• Study site — North Miami, Florida, United States
• Study site — Sunrise, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Augusta, Georgia, United States
• Study site — Roswell, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Marrero, Louisiana, United States
• Study site — Falls River, Massachusetts, United States
• Study site — Detroit, Michigan, United States
• Study site — Saginaw, Michigan, United States
• Study site — Lincoln, Nebraska, United States
• Study site — Lawrenceville, New Jersey, United States
• Study site — Neptune City, New Jersey, United States
• Study site — Plainsboro, New Jersey, United States

Full record on ClinicalTrials.gov

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