Assessment of Infection Control, Practice Efficiency, and Health Economics of Sheathed Versus Sta… (NCT02922868) | Clinical Trial Compass
CompletedNot Applicable
Assessment of Infection Control, Practice Efficiency, and Health Economics of Sheathed Versus Standard Cystoscopy
United States60 participantsStarted 2016-03
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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
What they're measuring
1
Number of Participants Who Had Post-Procedure Bacteriuria