Status:
COMPLETED
Investigation of the Ability of the TENA SmartCare Change Indicator to Reduce the Number of Manual Checks Between Changes of Absorbing Incontinence Products
Lead Sponsor:
Essity Hygiene and Health AB
Conditions:
Urinary Incontinence
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this post market clinical investigation is to demonstrate the performance and safety of the TENA SmartCare Change Indicator.
Detailed Description
The TENA SmartCare Change Indicator is intended for use on individuals, dependent end user (DEU), suffering from Urinary Incontinence (UI) who are cared for in a home environment, by one or more careg...
Eligibility Criteria
Inclusion
- DEU is diagnosed with urinary incontinence managed with a tape-style incontinence product.
- DEU is unable to sufficiently communicate the need for an incontinence product to be changed.
- DEU is being cared for in a home environment and most of the care is provided by a main CGR.
- DEU is willing and able to provide informed consent and to participate in the clinical investigation or has a legally designated representative willing to provide informed consent on behalf of the DEU. Note, the legally designated representative and main CGR cannot be the same person.
- CGR is willing and able to provide informed consent to participate in the clinical investigation.
- The CGR frequently checks the saturation level of the incontinence product, manually and/or by a touch-feel process.
- If incontinence is managed by pharmaceuticals, the dose regime is stable.
- DEU and CGR ≥ 18 years of age.
Exclusion
- DEU is cared for in a professional establishment or is institutionalized.
- DEU has ≥ 4 fecal "incidences" per week.
- DEU has severe incontinence product related skin problems, as judged by the investigator.
- DEU has any type of urinary catheter(s) resulting in improved/treated urinary incontinence.
- The incontinence product is changed on a routine based on time (schedule) or device alert, without manual checks.
- Any other condition that may make participation in the clinical investigation inappropriate, as judged by investigator.
- CGR is incapable or unwilling to use the required smart phone application and/or the diary registration webpage required for the clinical investigation.
- Participation in an investigational study of a drug, biologic, or device within 30 days prior to entering the clinical investigation or planned during the course of the clinical investigation.
- DEU is pregnant or nursing.
- CGR or DEU with an alcohol or drug addiction
Key Trial Info
Start Date :
April 14 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 28 2021
Estimated Enrollment :
35 Patients enrolled
Trial Details
Trial ID
NCT04846270
Start Date
April 14 2021
End Date
October 28 2021
Last Update
April 8 2024
Active Locations (1)
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1
Medical Concierge Centrum Medyczne
Warsaw, Poland, 02-798