Safety and Performance of a New 1-piece Ostomy Product Compared to Standard Care Ostomy Products in Subjects Ileostomy
Primary Purpose
Leakage, Skin Condition
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Standard Care
River
Sponsored by
About this trial
This is an interventional treatment trial for Leakage
Eligibility Criteria
List of Inclusion Criteria:
- Have given written informed consent.
- Are at least 18 years old.
- Have mental capacity to understand the study guidelines and questionnaires.
- Have had their ileostomy for at least 3 months
- Have an ileostomy with a diameter be-tween 19-40 mm.
- Are currently using a flat 1-piece product.
- Are able to change the product by them-selves or with help from a caregiver (e.g. spouse)
- Have experienced leakage under the base plate at least once a week over the last 2 weeks.
List of Exclusion criteria.
- Pregnant or breast-feeding.
- Currently receiving or have within the past 2 months received radio- and/or chemotherapy.
- Currently using topical steroid product on peristomal skin (injections and oral treatment are accepted).
- Are currently using a convex product
- Participating in other clinical studies or have previously participated in this study
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
River
Standard Care
Arm Description
Standard Care can have several manufacture and brand names. Standard Care is defined af the participants currently used stoma care product.
Outcomes
Primary Outcome Measures
Leakage underneath the baseplate
Secondary Outcome Measures
Peristomal skin condition
Measured by the Ostomy Skin Tool
Security
The participants feeling of security when wearing the product, measured on a 5-point scale
Handling
The participants ease of handling the products, measured on a 5-point scale
Comfort
The participants feeling of comfort when wearing the product, measured on a 5-point scale
Adverse events
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01448629
Brief Title
Safety and Performance of a New 1-piece Ostomy Product Compared to Standard Care Ostomy Products in Subjects Ileostomy
Official Title
An Open-labelled, Randomised, Controlled, Comparative, Explorative, Cross-over Study Investigating Safety and Performance of a New 1-piece Ostomy Product Compared Standard Care Ostomy Products in Subjects With Ileostomy
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Withdrawn
Why Stopped
The study was withdrawn because of problems found with the baseplate
Study Start Date
May 2011 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Coloplast A/S
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Introduction:
It is not an illness to have an ostomy, even though it is an indication of previous serious illness, such as cancer, which is the reason for approximately 80% of all ostomy operations. Ostomies can be divided into three categories: colostomy (large intestine), ileostomy (small intestine) and urostomy (urinary tract). All require surgical redirection of the intestine or urinary tract, allowing for elimination of urine and faeces by means of an opening in the abdominal wall. For the population included in this study, subject with an ileostomy, colitis ulcerosa is the main cause for an ileostomy where a surgical removal of the colon and rectum resulting in an ileostomy in theory cures the disease.
It can be very challenging to live with an ostomy and modern ostomy products should make life as easy as possible for people with ostomies.
Leakage and peristomal skin problems have been found to have a negative effect on the quality of life for people with ostomies. The skin problems are the reason for one out of three visits to ostomy nurses and occur much more frequently in people who have had ileostomies than in those who have had colostomies. It has been observed that the prevalence of peristomal skin problems is 21-60% among people who have ileostomies, 13-35% among those who have colostomies and 21-48% among those who have urostomies.
Leakage from ostomies that comes into contact with the skin is thought to predispose the patient to peristomal skin problems. One investigation of peristomal skin problems found that 77% of cases were related to contact with faeces or urine.
There are several reasons why leakage from an ostomy occurs, such as uneven peristomal area, improper handling of the ostomy product or a problematic ostomy (its formation, its location, retraction, prolapse or hernia). The ostomy may also change size with time, which can lead to leakage, if the ostomy products are not adapted accordingly. As a general rule, a check-up of the ostomy by an ostomy nurse or a doctor together with educational support can reduce these problems. Modern ostomy products should, however, also be constantly developed in order to lessen to the greatest extent possible the risk of leakage and associated inconveniences.
Detailed Description
See brief summary
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leakage, Skin Condition
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
River
Arm Type
Experimental
Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Standard Care can have several manufacture and brand names. Standard Care is defined af the participants currently used stoma care product.
Intervention Type
Device
Intervention Name(s)
Standard Care
Intervention Description
Participants are using their own product and this procedure is called "Standard Care".
Standard Care are the participants own products and may consist of several manufacturer and brand names.
Intervention Type
Device
Intervention Name(s)
River
Intervention Description
River is a new developed product with Coloplast as manufacturer
Primary Outcome Measure Information:
Title
Leakage underneath the baseplate
Time Frame
two weeks
Secondary Outcome Measure Information:
Title
Peristomal skin condition
Description
Measured by the Ostomy Skin Tool
Time Frame
Two weeks
Title
Security
Description
The participants feeling of security when wearing the product, measured on a 5-point scale
Time Frame
Two weeks
Title
Handling
Description
The participants ease of handling the products, measured on a 5-point scale
Time Frame
Two weeks
Title
Comfort
Description
The participants feeling of comfort when wearing the product, measured on a 5-point scale
Time Frame
Two weeks
Title
Adverse events
Time Frame
Two weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
List of Inclusion Criteria:
Have given written informed consent.
Are at least 18 years old.
Have mental capacity to understand the study guidelines and questionnaires.
Have had their ileostomy for at least 3 months
Have an ileostomy with a diameter be-tween 19-40 mm.
Are currently using a flat 1-piece product.
Are able to change the product by them-selves or with help from a caregiver (e.g. spouse)
Have experienced leakage under the base plate at least once a week over the last 2 weeks.
List of Exclusion criteria.
Pregnant or breast-feeding.
Currently receiving or have within the past 2 months received radio- and/or chemotherapy.
Currently using topical steroid product on peristomal skin (injections and oral treatment are accepted).
Are currently using a convex product
Participating in other clinical studies or have previously participated in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carol Katte, MD
Organizational Affiliation
Ashford and St. Peters Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Safety and Performance of a New 1-piece Ostomy Product Compared to Standard Care Ostomy Products in Subjects Ileostomy
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