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Assessment of the Performance of a New Ostomy Device in Subjects Having an Ileostomy

NCT03439241 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-06-06

No results posted yet for this study

Summary

The purpose was to investigate the performance of a new ostomy device measured with a measuring device.

Conditions

  • Ileostomy - Stoma

Interventions

DEVICE

Coloplast ostomy device

the test product is a newly developed Coloplast ostomy device

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Birte P Jakobsen, MD · Medical Director

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-05
Primary Completion
2018-04-16
Completion
2018-04-16

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 NCT03439241 on ClinicalTrials.gov