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Anti-infective Agent

Metronidazole 500 mg for Bacterial Vaginosis

Phase 4
Waitlist Available
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, approximately 9.5 months
Awards & highlights

Study Summary

This trial is testing whether the antibiotic metronidazole is effective in treating bacterial vaginosis (BV) in pregnant women.

Eligible Conditions
  • Bacterial Vaginosis

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, approximately 9.5 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, approximately 9.5 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Evaluating Composite of Chorioamnionitis, Postpartum Endometritis, SSI, Wound Infection, or Other Post-cesarean Infections (Occurring Within 6 Weeks After Delivery)
Secondary outcome measures
Evaluating Incidence of Adverse Events
Evaluating Incidence of Confirmed Sepsis for Newborns
Evaluating Incidence of Individual Infections.
+6 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Metronidazole 500 mgActive Control1 Intervention
Participants in this arm will receive metronidazole 500 mg twice daily, orally for 7 days
Group II: PlaceboPlacebo Group1 Intervention
Participants in this arm will receive placebo

Find a Location

Who is running the clinical trial?

Ohio State UniversityLead Sponsor
827 Previous Clinical Trials
502,735 Total Patients Enrolled

Frequently Asked Questions

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~4 spots leftby Apr 2025