Checking how accurately a glucose sensor measures sugar in adults with type 1 diabetes

Who can take part

• Adults who are 18-65 years of age, inclusive
• Patients with type 1 diabetes who use intensive insulin therapy (multiple daily injections (MDI) or continuous subcutaneous insulin infusion (CSII) including users of systems with continuous glucose monitoring (CGM) driven automatic adjustment of insulin doses for at least 3 months
• Patients who voluntarily decide to participate in the study and provide written informed consent

Who cannot take part

• Severe hypoglycemia events within 3 months prior to screening. Severe hypoglycemia is defined as loss of consciousness or seizure requiring emergency medical treatment due to hypoglycemia
• Participants with diabetic ketoacidosis within 3 months prior to screening
• History of epilepsy or syncope within 6 months prior to screening
• Patients who are currently participating or participated within 2 weeks prior to screening in another study or plan to participate in another study that in the opinion of the investigator would affect the safety of the study participant or the study result
• The following abnormal skin or skin diseases or skin alterations at the CGM sensor attachment or insertion site: Severe psoriasis, recent burn injury or severe sunburn, severe eczema, severe scar, extensive tattoo, dermatitis herpetiformis, severe rash, Staphylococcus aureus infection
• Allergic contact dermatitis to medical adhesives
• History of frequent catheter abscesses associated with pump therapy
• Conditions that predispose to hypoglycemia including inadequately treated thyroid and adrenal disease
• Unstable vascular diseases (defined by event or increasing symptoms in the last 6 months) or with insufficient therapy, including: Stroke, transitory cerebral ischemia, ischemic heart disease, peripheral vascular disease, and serious arrhythmia
• Patients with cognitive impairment or who are not suitable for this study or may be at increased risk associated with study participation in the opinion of the investigator
• Patients with anemia (hemoglobin below normal range)
• HbA1c >9.5%
• Hypoglycemia unawareness
• Patients scheduled for X-ray, MRI, CT or diathermy during the study
• Pregnant or lactating women or those who plan to become pregnant or do not agree to use an adequate method of contraception during the study
• Patients unwilling to abstain from ingesting the foodstuffs listed in Appendix 3 in excess of the allowed amounts
• Wearing of a pace maker or other comparable medical devices
• Dependency from the sponsor or the clinical investigator
• Unwillingness and/or inability to comply with study procedures