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Assessment of New Enhanced Ostomy Device in Real-life Settings in Subjects Having a Stoma

NCT03770078 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2025-04-01

Study results available
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Summary

The study investigates the performance of a new adhesive with regard to the skin condition

Conditions

  • Ileostomy - Stoma
  • Colostomy Stoma

Interventions

DEVICE

Test Product A

The test product is a newly developed ostomy product

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Birte P Jakobsen, MD · Consultant

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-12
Primary Completion
2019-03-06
Completion
2019-03-06

Countries

  • Denmark
  • Sweden

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 NCT03770078 on ClinicalTrials.gov