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NCT00945594 · ClinicalTrials.gov registry record · NA

Trial Comparing Outpatient Flexible to Rigid Cystoscopy in Females

A NA study, sponsored by University of Oklahoma.

Completed
Registry status
NA
Development phase
100
Enrollment target

NCT00945594: Completed NA study, sponsored by University of Oklahoma.

NCT00945594 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00945594, a NA study, has completed, sponsored by University of Oklahoma.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target

Study 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 time to resolution of these symptoms between the two procedures; to assess physician perception of patient pain or discomfort with flexible or rigid cystoscopy.

Primary Outcome

Post procedural complications, including frequency, urgency, infection and time to resolution of these symptoms between the two procedures. Patients were asked to report frequency or urgency as a "yes" or "no"

Interventions

  • DEVICE Cystoscopy

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2009-07
Est. Completion 2011-11
Phase NA
University of Oklahoma

358 total trials

What the finished NCT00945594 record still lists

NCT00945594 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Cystoscopy is the first listed.

NCT00945594 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00945594 about?

NCT00945594 is a clinical study titled "Trial Comparing Outpatient Flexible to Rigid Cystoscopy in Females". 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 time to resolution of these symptoms between the two procedures; to assess physician perception of p...

What is the current status of trial NCT00945594?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2009-07. Estimated completion is 2011-11.

What interventions are being tested in trial NCT00945594?

The interventions under investigation include: Cystoscopy (DEVICE).

Who is sponsoring clinical trial NCT00945594?

This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00945594's enrollment target sits among peer trials

100 840th of 2000 higher than 1,081 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00945594, the US trial registry maintained by the National Library of Medicine. NCT00945594 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.