Diabetes Mellitus
Conditions
Keywords
Non-invasive glucose monitoring, Raman spectroscopy
Brief summary
This explorative clinical study has been launched to collect spectral Raman data paired with validated glucose reference values in diabetic patients.
Detailed description
The Investigational Medical Device (IMD) for this investigation is the Prototype 0.5 (P0.5) developed and manufactured by RSP Systems (RSP). The device is intended for non-invasive interstitial intermittent glucose monitoring in persons (age 18 and older) with diabetes. The technology relies on the well-established capacities of Raman spectroscopy for directly detecting glucose subcutaneously. The Raman spectroscopy physical principle relies on the fact that when laser light of a given wavelength interferes with a molecule, a small fraction of the incident light will interact with the vibrational states of the molecule, causing the photons to lose a portion of their energy which will change the wavelength of the light. The scattered light will be collected by the optical probe head and analyzed with advanced algorithms to correlate the signal to glucose concentrations. Data collected from the IMD will be paired with validated glucose reference values collected by the finger sticking method.
Interventions
DEVICEPrototype 0.5
Investigational Medical Device collecting spectral Raman data from tissue
Sponsors
RSP Systems A/S
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male and female subjects ≥18 years of age * Diagnosed with diabetes, all types except gestational diabetes * HbA1c distribution \> 60 mmol/mol at baseline visit * 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 criteria
* 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 Danish * 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) * Reduced circulation in right hand evaluated by Allen's test * 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measurement accuracy of IMD | 4 months | Accuracy of measurements performed on the IMD will be evaluated by data from subjects. Data will be analyzed by Mean Absolute Relative Difference (MARD) and Inter Subject Unified Performance (ISUP) |
| Safety evaluation: paucity of adverse events | 4 months | Safety of the IMD will be evaluated in a descriptive manner by the paucity of adverse events reported during the clinical study |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Device deficiency | 4 months | Description of device deficiencies will be listed. Deficiencies will be reported during the clinical study. |
| Device usability | 4 months | The use of the device by the subjects will be evaluated by means of questionnaires |
Countries
Denmark
Outcome results
None listed