Safety, Tolerability and Efficacy of Vaginal Suppository WO3191 in the Post-treatment of Bacterial Vaginosis

NACompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

April 30, 2014

Primary Completion Date

July 31, 2015

Study Completion Date

September 30, 2015

Conditions
Vaginosis, Bacterial
Interventions
OTHER

Medical Device: WO3191

application of vaginal suppository WO3191: 2 days per week (with a treatment-free interval of three days or two days, respectively; e.g. Monday and Friday)

OTHER

Medical Device: Vagisan® Lactic Acid

application of Vagisan® Lactic Acid: 2 days per week (with a treatment-free interval of three days or two days, respectively; e.g. Monday and Friday)

Trial Locations (13)

Unknown

Dr. Gerick, Aachen

Dr. Hofmann, Betzdorf

Dr. de Brabandt, Bielefeld

Dr. Werner Göttker-Schnetmann, Frankfurt

Dr. Deininger, Munich

Dr. Kränzlin, Munich

Dr. Kästner, Munich

Dr. Kühne, Munich

Bianca Moll-Bosch, Siegen

Dr. Susanne Feidicker, Steinhagen

Thomas Riepen, Weilburg

Dr. Waldschütz, Wuppertal

Prof. Mendling, Wuppertal

All Listed Sponsors
collaborator

PHARMALOG Institute for Clinical Research

UNKNOWN

collaborator

Bremer Pharmacovigilance Service GmbH

OTHER

lead

Dr. August Wolff GmbH & Co. KG Arzneimittel

INDUSTRY