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Test of Discomfort and Malaise of Two Different Urine Catheters in Healthy Volunteers

NCT01142115 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2011-10-07

Study results available
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Summary

The purpose of this study is to evaluate the safety of a new developed catheter in comparison with an catheter on the market. The study is randomised.

Conditions

  • Spinal Cord Injury

Interventions

DEVICE

Intermittent catheter CP063CC

intermittent catheterisation

DEVICE

SpeediCath

intermittent catheterisation

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Rikke Otttesen, CTM · Coloplast A/S

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2010-05-31
Completion
2010-05-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01142115 on ClinicalTrials.gov