Status:
COMPLETED
Collecting Real-life Data for the Updated TENA SmartCare Change Indicator.
Lead Sponsor:
Essity Hygiene and Health AB
Conditions:
Urinary Incontinence
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This study is an explorative, open, single-arm clinical investigation to collect real-life measurement data in order to assess the mathematical algorithms involved in TENA SmartCare Change Indicator.
Detailed Description
The purpose of this exploratory clinical investigation is to evaluate safety and to collect real-life measurement data using the updated TENA SmartCare Change Indicator. The collected data will be use...
Eligibility Criteria
Inclusion
- Be willing and able to provide informed consent to participate or, if unable to provide such consent, have a legal representative who is willing and able to provide informed consent on behalf of the resident.
- Be 18 years of age of older.
- Be cared for at the investigation site.
- Suffer from urinary incontinence.
- Be current user of TENA Slip, Flex, Pants or Comfort incontinence products or during the course of the study be willing to become user of TENA Slip Flex, Pants or Comfort incontinence products.
- If applicable, be on a stable regimen of medications for urinary incontinence.
Exclusion
- Have frequent (daily) faecal incontinence in the pad or having severe problems with faecal incontinence as determined by the investigator.
- Have severe incontinence product related skin problems, as defined by the GLOBIAD categorization 2B (skin loss \& infection).
- Have any type of indwelling or external urinary catheter(s).
- Be anuric.
- Be of childbearing potential as determined by the investigator.
- Be managed using another automated or digital health technology incontinence management device.
- Have responsive behaviors of sufficient severity, in the opinion of the care staff, to make participation impractical.
- Have any other condition that makes participation in the clinical investigation
- Have a life expectancy of less than 90 days or be in receipt of palliative/terminal care.
- Have participated in an investigational study of a drug, biologic, or device within 30 days prior to entering the clinical investigation or planned during the clinical investigation.
- Be dependent on either alcohol or recreational drugs.
Key Trial Info
Start Date :
November 2 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 28 2024
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT06092099
Start Date
November 2 2023
End Date
February 28 2024
Last Update
March 15 2024
Active Locations (1)
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1
Tre Stiftelser Änggårdsbacken
Gothenburg, Sweden, SE-41346