Recurrent Bacterial Vaginosis and Vaginal Acidifying Gel Trial
Information source: Indiana University
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Bacterial Vaginosis
Intervention: Vaginal acidifying gel (RepHresh) (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Indiana University School of Medicine Official(s) and/or principal investigator(s): David M Haas, MD, Principal Investigator, Affiliation: Indiana University School of Medicine
Overall contact: David M Haas, MD, Phone: 3176307837, Email: dahaas@iupui.edu
Summary
Bacterial vaginosis (BV) is a common, complex clinical syndrome characterized by alterations
in the normal vaginal flora. Bacterial vaginosis has been associated with a variety of
adverse health outcomes including endometritis; post-abortion endometritis; nongonococcal,
nonchlamydial pelvic inflammatory disease; and an increased risk of acquiring and
transmitting HIV infection. In pregnancy, BV is associated with premature rupture of the
membranes, chorioamnionitis, amniotic fluid infection, preterm labor, preterm birth, and
postpartum endometritis. Several studies have documented increased postpartum complications
in the newborn and infants. The etiology of BV is poorly understood but recurrence is quite
common despite treatment. Documented recurrence rate of up to 30% within three months are
reported. Small studies have shown that adding vaginal acidifying gel to standard antibiotic
regimens may reduce recurrence rates of BV. We plan an RCT comparing standard antibiotic
therapy to antibiotics plus vaginal acidifying gel. Our hypothesis is that the addition of an
acidifying gel will decrease the chance of recurrence of BV within 3 months.
Clinical Details
Official title: Recurrent Bacterial Vaginosis (RBV): Efficiency of Metronidazole in Comparison to Metronidazole and Intravaginal Acidifying Gel: A Randomized Investigator-Blinded Controlled Trial
Study design: Treatment, Randomized, Single Blind (Outcomes Assessor), Parallel Assignment
Primary outcome: Recurrent bacterial vaginosis
Detailed description:
Women with recurrent BV will be randomly assigned to standard care of metronidazole vs
metronidazole plus vaginal acidifying gel. Symptoms and presence of BV will be measured at
followup.
Eligibility
Minimum age: 18 Years.
Maximum age: 50 Years.
Gender(s): Female.
Criteria:
Inclusion Criteria:
1. All women of between 18-50 years of age.
2. Confirmed current diagnosis of BV using Amsel's criteria.
3. Women with at least total 2 confirmed episodes of BV including most recent episode (by
Amsel's criteria) within a six month period or at least total three or more in the
past twelve months
Exclusion Criteria:
1. Patient who received antibiotic therapy within the past two weeks.
2. Patients who had co-existing gonorrhea or Chlamydia infection
3. Any contraindications or sensitivity to taking the vaginal gel.
4. Allergy to metronidazole
5. Alcoholics or those unable to abstain from alcohol consumption.
6. Pregnancy
Locations and Contacts
David M Haas, MD, Phone: 3176307837, Email: dahaas@iupui.edu
Indiana University School of Medicine, Indianapolis, Indiana 46202, United States; Recruiting David M Haas, MD, Principal Investigator
Additional Information
Starting date: September 2007
Ending date: July 2009
Last updated: July 31, 2008
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