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An Explorative Randomized Controlled Investigation Evaluating Newly Developed Ostomy Products

NCT02351817 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2016-01-06

Study results available
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Summary

The primary objective of the investigation is to explore the acceptance of a newly developed adhesive.

Conditions

  • Ileostomy

Interventions

DEVICE

Test A

Ostomy appliance

DEVICE

Test B

Ostomy appliance

DEVICE

Baseline

Ostomy appliance

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Birte Petersen Jakobsen, MD · Coloplast A/S

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2015-03-31
Completion
2015-03-31

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 NCT02351817 on ClinicalTrials.gov