CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 219 enrolled
Drug / intervention
SpeediCath +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00318591
NCT00318591N/ACompleted

A Prospective, Randomized, Parallel-group, Multi-center Study to Compare the Occurrence of Urinary Tract Infections in Patients With Spinal Cord Injury Using Either Coated or Uncoated Intermittent Catheters.

Coloplast A/S·interventional·Posted Apr 27, 2006·Updated Feb 10, 2021

In Brief

A clinical study evaluating SpeediCath and Conveen Uncoated for Urinary Tract Infections. Completed, enrolled 219 participants across 16 sites in 2 countries.

Detailed Summary

The purpose of this study is to investigate the frequency of urinary tract infections with symptoms in spinal cord injured patients requiring intermittent catheterization for emptying the bladder. Patients will use either a coated catheter or an uncoated catheter with gel.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 27, 2006
Enrollment StartApr 1, 2006
Primary CompletionOct 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 20.2 years ago

Interventions

SpeediCathdevice

hydrophilic coated urinary intermittent catheter

Conveen Uncoateddevice

Uncoated urinary intermittent catheter