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A Clinical Investigation of New Ostomy Appliances

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01523756
First Posted: February 1, 2012
Last Update Posted: March 10, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Coloplast A/S
  Purpose
This is an open-labelled randomized cross-over and controlled exploratory intervention that aims to include 20-30 patients with an ileostomy. Every patient is to test two new ostomy appliances each for two weeks. During the test a questionaire is to be filled out and interviews will take place. Primary parameter is leakage. A Study nurse will visit the participants in their homes every two week during the test.

Condition Intervention
Leakage Device: test product 1: new ostomy base plate with Coloplast as manufacturer Device: test product 2: new ostomy base plate with Coloplast as manufacturer

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Official Title: An Open-labelled Randomized Cross-over and Controlled Exploratory Investigation Comparing Several Variants of a Newly Developed Ostomy Appliance With Regard to Performance in 20 Patients With Ileostomy

Resource links provided by NLM:


Further study details as provided by Coloplast A/S:

Primary Outcome Measures:
  • Leakage Under the Base Plate Using a 24-point Scale [ Time Frame: Each product will be tested 2 weeks ]
    Leakage under the baseplate was measured with a 24 point scale where 0 points represents no leakage (best possible out come) and 24 points represents leakage on the whole plate (worst possible outcome)


Enrollment: 20
Study Start Date: February 2012
Study Completion Date: April 2012
Primary Completion Date: April 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: test product 1 first

own product (baseline) - test product 1 - test product 2

test product 1 = New ostomy base plate. Due to company confidentiality the product is just called test product 1

Device: test product 1: new ostomy base plate with Coloplast as manufacturer
test product 1 is tested first
Experimental: test product 2 first

own product (baseline) - test product 2 - test product 1

test product 2 = New ostomy base plate. Due to company confidentiality the product is just called test product 2

Device: test product 2: new ostomy base plate with Coloplast as manufacturer
test product 2 is tested first

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age > 18 years.
  2. Have had an ileostomy for more than 3 months.
  3. Have used convex products for the last 1 month.
  4. Has given written Informed Consent.
  5. Have an ileostomy with a diameter between 15 and 33 mm.
  6. Have inward peristomal area

Exclusion Criteria:

  1. Have loop ostomy
  2. Pregnant or breastfeeding.
  3. Known allergy towards any of the product components or ingredients.
  4. Currently receiving or have within the last 2 months received radio- and/or chemotherapy.
  5. Currently receiving or have within the past month received local or systemic steroid treatment in the peristomal area.
  6. Currently suffering from peristomal skin problems (i.e. bleeding or red and broken skin)
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01523756


Locations
Denmark
Coloplast A/S
Humlebaek, Denmark, 3050
Sponsors and Collaborators
Coloplast A/S
  More Information

Responsible Party: Coloplast A/S
ClinicalTrials.gov Identifier: NCT01523756     History of Changes
Other Study ID Numbers: CP226
First Submitted: January 10, 2012
First Posted: February 1, 2012
Results First Submitted: November 21, 2013
Results First Posted: March 10, 2014
Last Update Posted: March 10, 2014
Last Verified: January 2014