Using Phenazopyridine for In-office Cystoscopy

Status Active, not recruiting

Clinical Trial Summary

The investigators propose to conduct a randomized controlled trial to evaluate whether administration of phenazopyridine prior to the procedure decreases office cystoscopy time. Women undergoing in-office cystoscopy at Boston Urogynecology will be recruited.

Clinical Trial Description

All potentially eligible participants will have had a complete history, physical examination, urinalysis and urine culture for clinical purposes. After eligibility is confirmed and written, informed consent is obtained, participants will be randomized to one of the two study arms. Participants randomized to phenazopyridine arm will receive 200 mg by mouth approximately 60 minutes prior to the scheduled cystoscopy. During the cystoscopy, at various time points, the time will be recorded.The color of the efflux will also be documented. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02715648
Study type	Interventional
Source	Boston Urogynecology Associates
Contact
Status	Active, not recruiting
Phase	N/A
Start date	April 1, 2016
Completion date	June 1, 2021

View Details

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