Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04465682
Other study ID # Protocol CTP-Healthy.io-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 5, 2018
Est. completion date June 30, 2018

Study information

Verified date July 2020
Source Healthy.io Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Dip Home-Based Dipstick Analyzer (henceforth HBDA) is composed of a kit and a smartphone application. The device will be provided to the subject in a simulated home-use environment. All subjects will be asked to complete the urine test by following the application guidance, including providing a urine sample and scanning the urine strip after placing it on the Color-Board. The user will also complete a questionnaire to collect information regarding the use of the HBDA device. Following the usability test performed by the lay user, the subject's urine sample will be tested by the professional user using the comparator device. The use of the HBDA device will be evaluated for accuracy and identified risks. Additionally, measurable usability criteria for specific, critical steps will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date June 30, 2018
Est. primary completion date June 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Men and women 18-80 years of age

- Subjects who are healthy or pregnant; or

- Subjects diagnosed with a disease that normally represents itself with an abnormal concentration of one of the following urine analytes; Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Leukocytes, and Nitrite

- Subject is capable and willing to provide informed consent.

- Subject has facility with both hands.

- Subject is capable and willing to adhere to the study procedures

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Experimental: Dip Home-Based Dipstick Analyzer
Dip Home-Based Dipstick Analyzer The Dip Home-Based Dipstick Analyzer is a prescription, in-vitro diagnostic, home use device, which qualitatively and semi-quantitatively measures 10 urine analytes. The device combines a urine stick kit with an easy to use smartphone application using an image recognition algorithm.

Locations

Country Name City State
United States Atlanta Center for Medical Research Atlanta Georgia
United States AccuMed research associates Garden City New York
United States Activmed Practices & Research, Inc. Methuen Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Healthy.io Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of the % agreement of the Dip HBDA, tested by the lay user, as compared to a comparator device, tested by a professional user. 11 months
Secondary Evaluation of the Dip HBDA usability success rate, by potential lay users under actual use conditions 11 months
See also
  Status Clinical Trial Phase
Completed NCT04466774 - A Comparative, Controlled Study to Evaluate the Lay User Accuracy and Performance of the Dip Home-Based Dipstick Analyzer N/A