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Recruiting NCT05438199

Prototyping a Device for Automating Stool and Urine Output Tracking

No phase Interventional Waste Output

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Toilet seat that measures waste output.
Who it may be relevant to
Registry conditions: Waste Output. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of this study is to test an electronic apparatus for measuring stool and urine output in an accurate and easy way. Participants will have one in-person or virtual visit with the study team prior to starting the study events. Participants that enroll in this study will have the freedom to choose when to begin and stop using the toilet apparatus when it is available for human testing. This apparatus will be located in a private bathroom in either the CIEMAS building or MSRB III Building.

Interventions

  • Device Toilet seat that measures waste output
    Participants will use a toilet that includes a apparatus designed to measure waste output.

Primary outcome measures

  • Percent of urine output correctly identified as measured by toilet seat apparatus . [Time frame: Up to 3 months]
  • Percent of stool output correctly identified as measured by toilet seat apparatus . [Time frame: Up to 3 months]
Secondary outcome measures (2)
  • Percent of urine weight correctly identified by toilet seat apparatus [Time frame: Up to 3 months]
  • Percent of stool weight correctly identified by toilet seat apparatus [Time frame: Up to 3 months]

Eligibility criteria

Inclusion criteria

  • people who are able to use the private bathroom at no risk to themselves in the CIEMAS building (B508) or the bathroom located in room 4002, 4th floor of MSRB3.
  • students or employees at Duke University since card access is required for our MSRB3 bathroom.
  • people who spend most of their time in these buildings so we can assure the use of the toilet.
  • If the recruitment number is slow, enrollment will include people from the closest buildings.

Exclusion criteria

  • People who use wheelchairs or other mobility devices won't be able to enroll, since at this moment the bathroom is not compliant with the requirements on The Americans with Disabilities Act (ADA) of 1990.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Duke University — Durham

Identifiers

NCT: NCT05438199 · Pro00104899

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗