Scanadu Urine Device Validation Study Protocol
NCT02973178 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2016-11-25
Summary
This study will test Scanadu Urine Device for clinical performance and usability.
Conditions
- Urinary Tract Infections
- Proteinuria
- Ketone Urine
- Hematuria
- Glucose Intolerance
Interventions
- DEVICE
-
Scanadu Urine Device
Device to allow lay user to perform urinalysis test at home.
Sponsors & Collaborators
-
Scanadu, Inc.
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-08-31
- Primary Completion
- 2016-12-31
- Completion
- 2016-12-31
Countries
- United States
Study Locations
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