Biospecimen Analysis in Detecting Chemical Concentrations in Patients With Chronic or Infectious Diseases Receiving Meditations

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCity of Hope Medical Center

About this trial

This trial collects and analyzes sweat and saliva samples compared to blood in detecting chemical concentrations in the body in patients with chronic or infectious diseases receiving medications. Wearable sweat sensors are capable of monitoring electrolytes and metabolites (sodium, potassium, glucose, lactate, etc.) for health monitoring and disease diagnosis. Designing wearable sweat sensors capable of providing information regarding drug administration may be challenging due to ultralow concentrations in biofluids. This trial seeks to determine if the use of a smart wristband can accurately measure the levels of chemicals and substances in sweat.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Scheduled to receive medications including, but not limited to, cyclophosphamide, mycophenolic acid, mycophenolate mofetil, metformin or busulfan (any dose, any number of doses, any dosing frequency) as part of treatment at any time. Patients with chronic or infectious diseases can participate

Provide blood, sweat, and saliva samples

Permit medical record review

Disqualifiers

Pilocarpine allergy

Difficulty with understanding written English

Trial population

Patients with chronic or infectious diseases scheduled to receive medications

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Biospecimen Collection

    Procedure/Surgery

    Undergo collection of sweat, saliva, and blood samples

  • Medical Chart Review

    Other intervention

    Review of medical chart

  • Questionnaire Administration

    Other intervention

    Complete questionnaire

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Device feasibility (Macroduct Sweat Collection System)3 interventions

Trial outcomes

Primary outcomes

1

Predictive performance of the home-based sampling

Will be assessed by Pearson correlation and quantification of the predictive performance. The predictive performance of the home-based sampling methods will be assessed by calculating the median percentage prediction error (MPPE).

Time frame
Up to 4 hours
2

Observed plasma concentrations

Will be assessed by Pearson correlation and quantification of the predictive performance. The values from plasma will be considered the observed concentration.

Time frame
Up to 4 hours

Secondary outcomes

Other outcomes

Sponsors and contacts

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City of Hope Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator