Assessment of Infection Control, Practice Efficiency, and Health Economics of Sheathed Versus Standard Cystoscopy

Completed · Not applicable

Conditions studied: Bacteriuria

In brief

The purpose of this research study is to compare the effectiveness and efficiency of using a sterile sheath (EndoSheath®) during cystoscopy versus a standard scope.

Key facts

Study ID

NCT02922868

Run by

Wake Forest University Health Sciences

People needed

60

Starts

2016-03-01

Expected to finish

2016-12-01

Last updated by the study team

2018-09-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Males and females, at least 18 years of age or older
• Patients undergoing de novo or follow up diagnostic or therapeutic cystoscopy procedures in a Urology clinic setting
• Antibiotic-free for at least 7 days prior to cystoscopy procedure
• Patients willing to return to the clinic at approximately two weeks (10 -14 days) post-procedure for a urine test

You may not qualify if…

• Patients with significant lower urinary tract obstruction, gross hematuria
• Patients having an acute pelvic inflammatory disease or symptomatic UTI
• Patients with urethral strictures
• Patients with chronic pain conditions
• Patients unwilling to return to the clinic at approximately two weeks (10 -14 days) for a urine test

Where it is running

• Wake Forest Baptist Health - Department of Urology — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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