Product Evaluation of a Newly Developed Intermittent Catheter.

Coloplast

Status: Completed

Conditions: Incontinence, Urinary

Treatments: Device: Coloplast test catheter

Study type: Interventional

Funder types: Industry

Identifiers

NCT02966015

CP268

Details and patient eligibility

About

The aim of the study is to investigate the navigation of a newly developed catheter.

Enrollment: 153 patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male and at least 18 years
2. Has used Intermittent self-catheterization at least 3 months
3. Has normal to slightly reduced hand mobility
4. Use catheter size CH12 or CH14 (must use same size during product evaluation)

Exclusion criteria

1. Currently receiving treatment for urinary tract infection
2. Currently receiving chemotherapy

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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153 participants in 1 patient group

Testing the new Coloplast Test catheter

Experimental group

Description:

The subjects used the new Coloplast Test catheter for 1 week

Treatment:

Device: Coloplast test catheter