Testing a Device for Automatically TRacking Urine and STool in an Inpatient HCT Setting (Project TRUST)
Recruiting
N/A
Interventional Study
Fluid Output
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 80
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 54 (estimated)
- Sponsor
- Duke University · Other
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About This Trial
The purpose of this study is to determine whether a prototype toilet device that we have developed can accurately and automatically track human fluid output from renal and gastrointestinal systems in the hospital. The device includes components that can be outfitted onto existing toilets.
In this study, participants' hospital rooms will be outfitted with the prototype toilet device. Participants …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Scheduled to undergo an allogeneic or autologous hematopoietic stem cell transplant for any cancer or non-cancer illness through the Duke ABMT clinic OR currently undergoing treatment for HF in the Duke Cardiology Clinic with order of strict I/O monitoring
2. Age 18-80 years
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Contacts