Evaluation of an Incontinence Product

Hill-Rom

Status

Terminated

Conditions

Incontinence

Treatments

Other: Incontinence Detection System

Study type

Observational

Funder types

Industry

Identifiers

NCT03023072

CR-CWS2016-001

Details and patient eligibility

About

The purpose of this study is to determine if the sponsor's Incontinence Product reduces patient exposure time to a wet and/or soiled incontinence pad.

Enrollment

9 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

English speaking/reading adults, age ≥ 18 years
Incontinent (fecal, urine, or dual incontinence)
Patients with dual incontinence who require use of a fecal management system (but no urinary catheter)
Absence of skin irritation, breakdown, and pressure injuries present in the buttocks, sacrum, and/or perineal areas at the time of enrollment; minor irritation may be acceptable at the discretion of the Study Investigator
Willing and able to provide written informed consent or legal authorized representative is willing and able to provide written informed consent

Exclusion criteria

Presence of skin irritation and/or breakdown including but not limited to IAD or pressure injuries present in the buttocks, sacrum, and/or perineal areas at the time of enrollment; minor irritation may be acceptable at the discretion of the study Investigator
Require use of an absorbent undergarment (e.g. Depends) or catheter as the primary incontinence management strategy
Is considered to be near death or requires hospice care