A Study to Assess the Effectiveness of the Smart Water Bottle to Increase Fluid Intake in Patients with Kidney Stones and Low Urine Volume

Overview

About this study

The purpose of this study is to assess the effectiveness of the Smart Water Bottle technology to monitor and increase fluid intake in patients with kidney stones and low urine output.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • Age 18 or older
  • History of known kidney stone event (radiographic, passed, or treated)
  • Documented history of low urinary volume on at least one 24 hour urine analysis of <1.5L within past 6 months of potential enrollment
  • No planned changes to medication based on most recent 24 hour urine analysis

Exclusion Criteria

  • Cognitive impairment
  • Lack of smartphone
  • Coexisting medical condition that precludes high fluid intake such as chronic kidney disease, congestive heart failure, SIADH

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Mitchell Humphreys, M.D.

Closed for enrollment

Rochester, Minn.

Mayo Clinic principal investigator

Derek Gearman, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available
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CLS-20318082

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