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Liom Non-invasive Continuous Glucose Monitor "Clinical Demo" (niCGM)

Liom Non-invasive Continuous Glucose Monitor "Clinical Demo" (niCGM)

Recruiting
18-65 years
All
Phase N/A

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Overview

This is a single-centre, multiple cohort, open study.

Description

The study will include 5 cohorts. After each cohort, optimisation of the Spiden Clinical Demo 2.0 system and machine learning models may be pursued before the next cohort is started. Trial participants with type 1 or type 2 diabetes mellitus.

Eligibility

Inclusion Criteria:

  • Male or female trial participant with clinically diagnosed type 1 or type 2 diabetes for at least 1 year.
  • Age between 18 and 65 years, both inclusive.
  • Treated with insulin and/or oral antidiabetic drugs (OADs; type 2 only), multiple dosing insulin therapy (MDI), continuous subcutaneous insulin infusion (CSII) or a hybrid closed loop system.

Exclusion Criteria:

  • Known or suspected hypersensitivity to any of the components of the Liom Clinical Demo 2.0.
  • Trial participant with any injury, infection, atypical skin condition (e.g., hyperkeratosis, hyperpigmentation) of or tattoo on the wrists.
  • Presence or history of a cardiovascular disease including stable and unstable angina pectoris, myocardial infarction, transient ischaemic attack, stroke, cardiac decompensation, clinically significant arrhythmias or clinically significant conduction disorders.

Study details
    Type 1 Diabetes
    Type2diabetes

NCT06272136

Liom Health AG

21 October 2025

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