CGM Experience, Preferences & Blood Glucose Parameters

Inclusion Criteria:

• Subjects to provide written informed consent prior to any study procedures being performed
• Subjects with age 18 and above both male and female
• Diagnosed with Diabetes Miletus Type I, Type II and/or GDM
• Comfortable using smart phone, access to internet along with Bluetooth connectivity throughout the study duration.
• Subjects (Patients) on oral or injectable anti-diabetic medications, (in case of insulin, patient must be on insulin from last 3 months )
• Subjects (HCPs) healthy, Pre-diabetes or Diabetes Miletus (any type)

Exclusion Criteria:

• History of hypersensitivity to any of the active or inactive ingredients of the CGM device used in the trial, and/or history of significant allergic skin reactions.
• Presence of severe diabetes complications e.g. retinopathy, acute metabolic crisis, etc.
• History of active/ acute renal and/or hepatic failure.
• Patients who have been admitted to the hospital in the past 3 months for diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state.
• History of critical illness or incapacitated patients
• History of acute psychiatric disorder or exacerbation of chronic psychiatric disorder.
• History or presence of a medical condition or disease that in the investigator's opinion would embarrass glycemic control and completion of the study.
• Medical conditions that require patients to undergo frequent radiation/ imaging procedures for example CT, MRI and X rays
• History of known hematological disorders such as Sickle Cell Disease & Trait, Thalassemia, Hemolytic Anemias (e.g., G6PD deficiency, autoimmune), Iron Deficiency Anemia
• Patients on high doses of acetaminophen (>1 gram every 6 hours), ascorbic acid supplements (e.g., > 500-1000 mg/day), IV sorbitol, steroids and aspirin which can alter the readings on the CGM device.