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Clinical Study Evaluating Safety of a New Catheter for Urinary Intermittent Catheter in Healthy Volunteers

NCT01292941 · Status: WITHDRAWN · Phase: PHASE1 · Type: INTERVENTIONAL

Last updated 2015-08-07

No results posted yet for this study

Summary

To evaluate discomfort of a new coating and catheter material compared to SpeediCath (SC)

Conditions

  • Spinal Cord Injury

Interventions

DEVICE

Intermittent catheterisation

Speedicath, Intermittent catheterisation

DEVICE

NonCE marked intermittent catheter/red

Paris, Intermittent catheterisation

DEVICE

NonCE marked intermittent catheter/green

Paris, Intermittent catheter

DEVICE

NonCE marked intermittent catheter/blue

Paris, Intermittent catheter

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Susanne Gürtler, CTM · Coloplast A/S

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2011-06-30
Completion
2011-06-30

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 NCT01292941 on ClinicalTrials.gov