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A Clinical Data Collection Study of Verily Patch

A Clinical Data Collection Study of Verily Patch

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04727801
Enrollment
22
Registered
2021-01-27
Start date
2021-03-11
Completion date
2021-05-25
Last updated
2021-08-20

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

Conditions

Afebrile, Febrile

Brief summary

This is a single center, prospective, non-randomized prospective observational data collection study of the Verily Patch. The Verily Patch is an investigational wearable, continuous temperature sensor which will be evaluated against reference oral and axillary temperature measurements to support development activities for the Verily Patch.

Interventions

DEVICEVerily Patch

The Verily Patch is an investigational wearable temperature sensor that consists of a Patch (Verily Patch), with swappable adhesives, as well as an app (Verily Patch app).

Sponsors

Verily Life Sciences LLC
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* At least 18 years old * Able to read and speak English * Able to read and understand the Informed Consent Form * Willing to wear Verily Patch in the axillary region * Willing to comply with repeated self-measurement of oral and axillary temperatures and willing to record temperature readings * Have a working smartphone device and willing to use it for study activities * Willing to install study apps on their personal smartphone * Willing to comply with all study-related procedures

Exclusion criteria

* Pregnant or breastfeeding during study participation * Have known allergies to medical grade adhesives * Have known cutaneous hypersensitivity * Have infection in both axilla * Have open injury or rash where the study device will be worn * Have a cardiac pacemaker or other implanted electronic medical device(s) * Have any additional condition or situation that, in the opinion of the investigator, makes the subject inappropriate for participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Data collection to support development activities for Verily PatchUp to 8 daysData collection to enable device development of the Verily Patch, which includes the development of an algorithm that estimates temperature

Countries

United States

Outcome results

None listed

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