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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 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 100 participants.
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.
Interventions
- DEVICE Cystoscopy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2009-07 |
| Est. Completion | 2011-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00945594
The ClinicalTrials.gov registry entry for NCT00945594 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Cystoscopy is the first listed.
NCT00945594 reports 0 study locations.
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.
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