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NCT05874635

Signos DM2 Empowerment Study (SIGNOS-CGM-EMPOWER-201-2022)

Active, enrolled NA Last updated 29 August 2025
What this trial tests

NA trial testing Continuous Glucose Monitor Device in Weight Loss in 20,000 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
11 May 2023
Primary endpoint
10 May 2028
10 May 2029

Quick facts

Lead sponsorSignos Inc
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20,000
Start date11 May 2023
Primary completion10 May 2028
Estimated completion10 May 2029
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Signos Inc

Who can join

18 and older, any sex, with Weight Loss or Metabolic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The use of continuous glucose monitoring (CGM) in earlier data has inspired behavioral changes leading to improved adherence to an exercise plan in individuals and eating habits in people with diabetes. Mobile health (mHealth) platforms provide satisfactory, easy-to-use tools to help participants in the pursuit of weight change goals. We hypothesize that the use of CGM data and the Signos mHealth platform will assist with weight control in a population of people with type 2 diabetes mellitus who are not using insulin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Continuous Glucose Monitor Device

Trials testing the same drug.

Other recruiting trials for Weight Loss

Currently open trials in the same condition.

Other Signos Inc trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05874635.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing