Collaborative Urological Prosthetics Investigation Directive Research Group

EARLY_PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

800

Participants

Timeline

Start Date

April 22, 2022

Primary Completion Date

December 31, 2025

Study Completion Date

January 1, 2026

Conditions
Erectile DysfunctionPenile Prosthesis Infection
Interventions
DRUG

Doxycycline

Patients will be given 6 days of oral antibiotics based on local biograms, patient allergies and renal and liver function

DRUG

Ciprofloxacin

Patients will be given 6 days of oral antibiotics based on local biograms, patient allergies and renal and liver function

DRUG

Augmentin

Patients will be given 6 days of oral antibiotics based on local biograms, patient allergies and renal and liver function

DRUG

Bactrim

Patients will be given 6 days of oral antibiotics based on local biograms, patient allergies and renal and liver function

Trial Locations (1)

60637

University of Chicago, Chicago

All Listed Sponsors
collaborator

Loyola University

OTHER

lead

University of Chicago

OTHER