Glucose monitoring by wearable watch

Feasibility for the use of a non-invasive wearable device for glucose monitoring. - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071227

Enrollment

1000

Registered

2024-07-24

Start date

Unknown

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Health Condition 1: E11- Type 2 diabetes mellitus

Interventions

Intervention1: LUMOS wearable device: A fingertip version of the LUMOS device uses non-invasive optical spectroscopy to determine physiological responses of the fingertip. The device will noninvasivel

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age of 18 years or older. 2. Ability to provide informed consent. 3. Reports having a secure place to store an electronic device.

Exclusion criteria

Exclusion criteria: 1. Inability to consent. 2. Presence of hand tattoos or markings that could interfere with the optical sensor.

Design outcomes

Primary

Measure	Time frame
Determining whether it is feasibleTimepoint: 2 months	—

Secondary

Measure	Time frame
Determining whether it is acceptable.Timepoint: 1 week	—

Countries

India

Contacts

Public ContactDr S Poongothai

Madras Diabetes Research Foundation

drmohans@diabetes.ind.in04443968888

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026