Status:

WITHDRAWN

Performance and Safety Evaluation of a Novel Non-invasive Glucose Monitoring Device

Lead Sponsor:

RSP Systems A/S

Conditions:

Diabetes Mellitus

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This pivotal multicenter study has been launched to collect spectral Raman data paired with validated glucose reference values in diabetic patients.

Detailed Description

Participants will be enrolled at six different sites in four different countries. All participants will undergo identical procedures, which include four steps: Baseline visit (1 day), calibration peri...

Eligibility Criteria

Inclusion

  • Male and female subjects ≥18 years of age
  • Diagnosed with diabetes, all types except gestational diabetes
  • Skin phototype 1-4
  • Willing to perform a minimum of 8 finger sticks during each day of home-based measurements and 30 finger sticks at the two in-clinic study days
  • Subject has a wireless internet connection at home to be used in the study

Exclusion

  • For female subjects: Pregnancy or subject is attempting to conceive or not willing and able to practice birth control during the study duration
  • For female subjects: Breastfeeding
  • Subject currently participating in another study
  • Subject not able to understand and read the local language
  • In investigator's opinion, subject is not able to follow instructions provided and as specified in the protocol
  • Subject not able to hold hand/arm steady (including tremors and Parkinson's Disease)
  • Subject diagnosed with cardiovascular diseases
  • Reduced circulation in right hand evaluated by Allen's test
  • Subjects receiving anticoagulants, active cancer treatment, tetracyclines and other medication/topical agents increasing photosensitivity
  • Radiotherapy for the past six months
  • Extensive skin changes, tattoos or diseases on right hand thenar (probe application site)
  • Known allergy to medical grade alcohol used to clean the skin
  • Medical history or any condition that may, in the opinion of the investigator compromise the subject's ability to participate
  • Comorbidity or concomitant medical condition which, in the opinion of the Investigator, could interfere with the study or present a risk to the safety or welfare of the subject or study staff

Key Trial Info

Start Date :

June 1 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2019

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT04031300

Start Date

June 1 2019

End Date

June 1 2019

Last Update

November 21 2023

Active Locations (6)

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Page 1 of 2 (6 locations)

1

Steno Diabetes Center Copenhagen (SDCC)

Gentofte Municipality, Denmark, 2820

2

Steno Diabetes Center Odense (SDCO)

Odense C, Denmark, 5000

3

Institut für Diabetes-Technologie Forschungs- und Entwicklungs-gesellschaft mbH an der Universität Ulm (IDT)

Ulm, Germany, 89081

4

Sahlgrenske University Hospital (SUH)

Gothenburg, Sweden, 413 45

Performance and Safety Evaluation of a Novel Non-invasive Glucose Monitoring Device | DecenTrialz