To determine the safety profile of sodium fluorescein in women undergoing cystoscopy during
gynecologic surgery. To determine if either oral phenazopyridine or sodium fluorescein result
in shorter cystoscopy times.
Drug: sodium fluorescein
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Locations near you
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Full eligibility criteria for NCT02757417
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
- Patients must be 18 years or older as well as willing and able to provide informed consent
Patients undergoing a scheduled gynecologic procedure with cystoscopy
- Patients are younger than 18 years
Patients are unable or unwilling to provide informed consent
Patients with a history of an allergic reaction to sodium fluorescein or phenazopyridine
Patients with a history of renal insufficiency
Patients with a history of liver disease
Patients with a history of sickle cell disease
Patients with a history of glucose-6-phosphate dehydrogenase deficiency
Patients with a history of chronic obstructive pulmonary disease or currently being treated for asthma
All locations for NCT02757417
United States (1)
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States, 44106
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View full eligibility
Tris trial is registered with FDA with number: NCT02757417. The sponsor of the trial is University Hospitals Cleveland Medical Center and it is looking for 88 volunteers for the current phase.
Official trial title: A Randomized Trial Comparing Intaoperative Intravenous Sodium Fluorescein to Pre-Operative Oral Phenazopyridine For Evaluation of Ureteral Patency
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