Phenazopyridine for Confirmation of Ureteral Patency
Completed · Not applicable
Conditions studied: Cystoscopy
In brief
In this prospective, randomized trial subjects will be randomized to receive phenazopyridine or no medication prior to pelvic reconstructive procedures that use cystoscopy to confirm ureteral patency intraoperatively.
Key facts
- Study ID
- NCT02424149
- Run by
- Hartford Hospital
- People needed
- 107
- Starts
- 2015-04-01
- Expected to finish
- 2016-01-01
- Last updated by the study team
- 2016-12-05
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Females only
- Planned surgical procedure where cystoscopy will be used to document ureteral urine flow
- Age > or = 18 years, no upper age limit
- Able and willing to consent
You may not qualify if…
- Planned surgical procedure where cystoscopy will not be used
- Planned surgical procedure where cystoscopy is used for a purpose other than documenting ureteral urine flow
- age <18 years
- pregnancy
- unable/unwilling to participate
- history of allergy or adverse reaction to phenazopyridine
- hepatic dysfunction
- known phenazopyridine hypersensitivity
- history of urologic surgery
- presence of ureteral stents prior to the planned surgical procedure
- concomitant suprapubic catheter placement
Where it is running
- Hartford Hospital — Hartford, Connecticut, United States
Full record on ClinicalTrials.gov
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