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Study of Metabolic Content of Urine

Longitudinal Study of Metabolic Content of Human Urine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05637840
Enrollment
25
Registered
2022-12-05
Start date
2022-12-06
Completion date
2023-11-18
Last updated
2024-02-16

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

Conditions

Metabolic Content of Urine

Brief summary

The purpose of this research study is to test the different components in urine and see if they can be matched to food, exercise and sleep that participants report. The researchers are trying to find out if urine would allow them to predict medical problems as they are happening. Participants are healthy volunteers who are willing to give urine samples on a daily basis, and can expect to be in the study for 28 days.

Detailed description

The purpose of this research study is to analyze urine samples using Mass Spectrometry to identify metabolites that have the potential to be used for medical diagnosis. This data, along with data from wearable devices, will be combined and analyzed to correlate what an individual does on a daily basis with how their body metabolizes their choices. This type of data may provide insights into the origins and progression of diseases in a short time span.

Interventions

OTHERUrine sample

Collection of 36-84 urine samples over a 14 consecutive day period.

OTHERSleep restriction

Participants will be asked to limit their sleep to 4 hours within a 24-hour period for 2 days in a row.

Sponsors

Morgridge Institute for Research
CollaboratorUNKNOWN
University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Must be 18 years or older * Be able to provide informed consent * Stated willingness to comply with all study procedures and have availability for the duration of the study

Exclusion criteria

* Presence of a condition(s) or diagnosis, either physical or psychological, that limits the ability to urinate in the collection apparatus * Individuals who do not consistently get at least 6 hours of sleep per night * Individuals who have a sleep disorder diagnosis. * Individuals who live in the state of New York

Design outcomes

Primary

MeasureTime frameDescription
Change in inflammationBaseline to day 14Changes in inflammation will be measured by hs-CRP via short-term sleep restriction.
Correlate biohealth data with concentrations of urine metabolitesDaily for 14 daysTo explore connections between urine metabolite concentrations and others measures of health and lifestyle, biometric data will be collected using a FitBit watch (sleep and exercise), nutritional data (food logs) and a questionnaire (tobacco use). Urine will be analyzed using mass spectrometry to isolate metabolites. The metabolites will then be cross-referenced against databases of known metabolites in order to identify them and their disease associations.

Countries

United States

Outcome results

None listed

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