MedTrace Logo

Sharklet Catheter Study

NCT02669342 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2017-04-06

No results posted yet for this study

Summary

The aim of this study is to determine if the Sharklet catheter, with its unique coating, reduces infections in participants, when compared to a standard catheter.

Conditions

Interventions

DEVICE

Radiance™ Clear Sharklet® Silicone Foley Catheter

DEVICE

Silicone Foley Catheter

Sponsors & Collaborators

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Dirk Lange, PhD · University of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2019-02-28
Completion
2019-02-28

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT02669342 on ClinicalTrials.gov