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RECRUITING
NCT06706362
PHASE4

Assessing the Utility of Prophylactic Antibiotics at Time of Urethral Bulking Using Bulkamid (Bulkamid Study)

Sponsor: Ohio State University

View on ClinicalTrials.gov

Summary

The primary aim of this study is to assess the utility of prophylactic oral antibiotics at time of Bulkamid transurethral bulking to reduce the incidence of urinary tract infection (UTI) in the immediate postoperative period. The secondary aims of the study include assessing UTI rates and success rates if patients require temporary indwelling catheter versus intermittent self-catheterization (ISC).

Official title: Assessing the Utility of Prophylactic Antibiotics at Time of Urethral Bulking Using Bulkamid

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

138

Start Date

2025-09-15

Completion Date

2027-10-15

Last Updated

2025-10-08

Healthy Volunteers

No

Interventions

DRUG

Bactrim or Macrobid

Participants will be assigned to Bactrim or Macrobid depending on participants' allergies

DRUG

Placebo

Participants will be assigned to identical appearing placebo

Locations (1)

The Ohio State University Wexner Medical Center OB/GYN Female Pelvic Medicine and Reconstructive Surgery

Columbus, Ohio, United States