Status:
COMPLETED
Trial Comparing Outpatient Flexible to Rigid Cystoscopy in Females
Lead Sponsor:
University of Oklahoma
Conditions:
Pain
Eligibility:
FEMALE
18-99 years
Phase:
NA
Brief Summary
The primary purpose of this study to assess patient pain scores comparing rigid to flexible cystoscopy in females; to assess post procedural complications, including frequency, urgency, infection and ...
Detailed Description
This will be a prospective randomized trial study in order to determine to compare rigid and flexible cystoscopy in female patients. Patients will be recruited from OU Physicians Pelvic and Bladder He...
Eligibility Criteria
Inclusion
- Patients with the following indications for outpatient cystourethroscopy:
- Microscopic hematuria or
- Voiding dysfunction, or recurrence of urinary incontinence, or
- History of recurrent bacterial cystitis
- Age \>18
- Patient willingness to enroll
- Patient able to read and understand an English language self- administered questionnaire.
Exclusion
- Severe detrussor overactivity
- Interstitial cystitis or chronic urethral or bladder pain
- Acute urinary tract infection
- Urinary retention defined as a post void residual \>120cc
- Pregnancy or planning pregnancy within the next 3 months
- Prior urethral surgery
- Dementia or inability to complete questionnaires
Key Trial Info
Start Date :
July 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2011
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00945594
Start Date
July 1 2009
End Date
November 1 2011
Last Update
June 6 2019
Active Locations (1)
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1
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States, 73104