To Determine the Efficacy of Irrisept in Reducing Urinary Tract Infection During Urethral Catheter Removal.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Given the high burden of post-catheter removal UTIs, this study aims to evaluate Irrisept instillation as a non-antibiotic intervention to reduce infection rates. By comparing Irrisept to saline irrigation, the study will provide critical insights into the efficacy of antiseptic bladder irrigation in preventing UTIs while minimizing antibiotic use. If successful, this approach could lead to new clinical guidelines for catheter removal protocols, improving patient outcomes and reducing healthcare costs.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Presenting to the urology clinic for catheter removal

• Must be 18 years or older.

• The patient must be able to understand and willing to provide informed consent as described in this study protocol.

• Must be willing to complete a post-catheter removal survey

Locations
United States
Ohio
The Ohio State University
RECRUITING
Columbus
Time Frame
Start Date: 2025-12-31
Estimated Completion Date: 2028-01-01
Participants
Target number of participants: 300
Treatments
Active_comparator: Control
Standard of care
Experimental: Experimental
Experimental
Related Therapeutic Areas
Sponsors
Collaborators: Irrimax Corporation
Leads: Ohio State University

This content was sourced from clinicaltrials.gov