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Skin Problems in Ostomy Patients: An Epidemiological Study

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2006 by Roskilde County Hospital.
Recruitment status was  Active, not recruiting
Sponsor:
Collaborator:
Coloplast A/S
Information provided by:
Roskilde County Hospital
ClinicalTrials.gov Identifier:
NCT00391508
First received: October 23, 2006
Last updated: NA
Last verified: October 2006
History: No changes posted
  Purpose

Peristomal skin complications are thought to be common but the exact frequency and cause of these complications are unknown. We have sought to document the incidence of cutaneous peristomal problems and to find risk factors that might contribute to peristomal complications.


Condition
Ostomy
Living in Roskilde County
Persons More Than 18 Years of Age
Willingness to Participate

Study Type: Observational
Study Design: Observational Model: Case Control
Primary Purpose: Screening
Time Perspective: Cross-Sectional
Official Title: An Epidemiological Study of Peristomal Skin Problems in Patient With an Ostomy in Roskilde County

Resource links provided by NLM:


Further study details as provided by Roskilde County Hospital:

Estimated Enrollment: 200
Study Start Date: September 2003
Estimated Study Completion Date: August 2005
Detailed Description:

Peristomal skin complications are thought to be common but the exact frequency and cause of these complications are unknown. We have sought to document the incidence of cutaneous peristomal problems and to find risk factors that might contribute to peristomal complications.

A cross sectional study was conducted from September 2003 to January 2005. The study population included all persons with an ostomy living in Roskilde County, Denmark. We have attempted to include all persons with an ostomy by contacting the local municipalities administering individual aid. Danish law (law of social service section 4 chapter 19 § 97) states that every person with a chronic disease is entitled to reimbursement for any aid needed. For ostomy patients this means that they are entitled to free stoma care products from selected merchants and without restriction to type or manufacturer of ostomy product. All ostomy patients are automatically enrolled in the database at the local municipality in order to received reimbursement for product cost. It was therefore assumed that all ostomy patients were registered, as the law provides benefits without restrictions, and self-payment for alternative purchases would involve substantial additional and unnecessary private expenditure for the individual ostomy patient.

A letter was sent to every ostomy patient by the municipalities, inviting them to participate. The ostomy patients willing to participate would then return the stamped and addressed envelope with their reply. For all patients who accepted the invitation, a physical examination was scheduled.

At the time of the examination a detailed registration form was filled out to provide standardised records of known risk factors and other data of possible pertinence to the investigation.

A careful physical examination was performed by a dermatologist, a stoma care nurse specialist and a resident. The majority of ostomy patients were seen at the dermatological department Roskilde University Hospital, but a few were seen at their homes due to advanced age or physical impairment. Personal details, medical histories, stoma appliances and daily stoma care routines were recorded along with a thorough examination of the peristomal area in regards to ostomy placemant, skin retraction, hernia, stoma height and width. A general skin examination was also undertaken. Each variable was recorded and further documented by colour photographs. To ensure that the participating patients correlated to the general population, a national computer based register of all ostomy patients in Denmark were compared to our patients in regards to ostomy type, sex, age and geographical location. Patients with a peristomal skin problem and a control (person without a skin problem) were selected from the cross-sectional study and invited for further examination. At this examination several non invasive test were conducted. These non invasive test included: D-squame tapes, Capacitans measurements , TEWL(transepidermal water loss) measurements , Tape stripping, Mecanical measurements of the skin and pH measurements.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Ostomy
  • Living in Roskilde County
  • Persons more than 18 years of age
  • Willingness to participate

Exclusion Criteria:

  • Under 18 years of age
  • Living outside Roskilde County
  • If not able to comprehend the study
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00391508

Locations
Denmark
Roskilde University Hospital, Dept. of Dermatology
DK-4000 Roskilde, Denmark, 4000
Sponsors and Collaborators
Roskilde County Hospital
Coloplast A/S
Investigators
Principal Investigator: Hanne Nybaek, MD Dept. of Dermatology, Roskilde Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00391508     History of Changes
Other Study ID Numbers: Sept-HN-2003
Study First Received: October 23, 2006
Last Updated: October 23, 2006
Health Authority: Denmark: Ethics Committee

Keywords provided by Roskilde County Hospital:
Ostomy
Peristomal skin
Skin complication

ClinicalTrials.gov processed this record on November 25, 2014