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Impact of Sterilization Technique on Incidence of Urinary Tract Infection After Cystoscopy

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00177112
First Posted: September 15, 2005
Last Update Posted: February 4, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Minnesota - Clinical and Translational Science Institute
  Purpose
The purpose of this study is to verify that the incidence rate of urinary tract infections after a routine outpatient cystoscopy is the same for non-sterile (clean) and sterile procedural techniques.

Condition Intervention Phase
Urinary Tract Infections Procedure: clean patient preparation for cystoscopy Procedure: sterile patient preparation for cystoscopy Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Impact of Sterilization Technique on Incidence of Urinary Tract Infection After Cystoscopy

Resource links provided by NLM:


Further study details as provided by University of Minnesota - Clinical and Translational Science Institute:

Primary Outcome Measures:
  • To verify that the incidence rate of urinary tract infections after a routine outpatient cystoscopy is the same for non-sterile (clean) and sterile procedural techniques

Estimated Enrollment: 275
Study Start Date: June 2005
Study Completion Date: October 2007
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 18 years of age or older
  • Patients undergoing routine outpatient flexible cystoscopy

Exclusion Criteria:

  • Patients who have had a urinary tract infection within 3 months prior to flexible cystoscopy
  • Patients with an indwelling catheter
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00177112


Locations
United States, Minnesota
VAMC Minneapolis
Minneapolis, Minnesota, United States, 55417
Sponsors and Collaborators
University of Minnesota - Clinical and Translational Science Institute
Investigators
Principal Investigator: Kyle Anderson, MD VAMC Minneapolis
  More Information

Responsible Party: Manoj Monga, MD, University of Minnesota
ClinicalTrials.gov Identifier: NCT00177112     History of Changes
Other Study ID Numbers: 0412M65852
3519A
First Submitted: September 13, 2005
First Posted: September 15, 2005
Last Update Posted: February 4, 2008
Last Verified: January 2008

Keywords provided by University of Minnesota - Clinical and Translational Science Institute:
Cystoscopy

Additional relevant MeSH terms:
Infection
Communicable Diseases
Urinary Tract Infections
Urologic Diseases
Disinfectants
Anti-Infective Agents