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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Withdrawn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
Coloplast A/S
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Leakage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    August 18, 2011
    Last Updated
    February 6, 2012
    Sponsor
    Coloplast A/S
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    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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