Incontinence Management System ICU Field Evaluation

Hill-Rom Incontinence Management System ICU Field Evaluation

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03628833

Enrollment

Registered

2018-08-14

Start date

2018-07-10

Completion date

2018-12-03

Last updated

2019-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fecal Incontinence, Urinary Incontinence

Brief summary

The objective of this Field Evaluation is to assess usage and satisfaction associated with the Hill-Rom Incontinence Management System.

Interventions

DEVICEIncontinence Management System

Incontinence detection device

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patients with urinary, fecal, or dual incontinence who are ≥ 18 years old * The patient, or the patient's legal authorized representative (LAR), is willing and able to provide written informed consent

Exclusion criteria

\- Patients that are considered to be near death or require palliative care

Design outcomes

Primary

Measure	Time frame	Description
Staff satisfaction surveys on product performance	Through study completion, an average of 4 months	Following product use, staff can complete an optional, Likert scale survey

Secondary

Measure	Time frame
Patient exposure time following an incontinence event	Through study completion, an average of 4 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026