Can a glucose monitor boost diabetes remission? new trial aims to find out

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18-75 years old * T2D treated with ≤ 3 non-insulin antihyperglycemic agents * A clinical diagnosis of T2D for \> 6 months and ≤ 6 years ago * HbA1c 6.0-9.0% on 2 or 3 antihyperglycemic agents, HbA1c 6.5-9.0% on 1 antihyperglycemic agent, or HbA1c 7.0-9.0% on 0 antihyperglycemic agents * BMI 27-44.9 kg/m2 * Not currently using a real-time CGM or isCGM * Willing to adhere to LCMR and initiate isCGM or CBG monitoring, and capable to do so as judged by investigator Exclusion Criteria: * Current or prior use of insulin (except for prior management of gestational diabetes mellitus) * Are pregnant or breastfeeding, or planning to become pregnant in the next 2 years * Severe or progressive retinopathy * Have a history of cardiovascular disease: coronary artery disease (CAD): prior myocardial infarction, previous unstable angina, documented CAD on angiography with stenosis \>50%, imaging evidence of myocardial ischemia, coronary revascularization), peripheral arterial disease (lower extremity stenosis exceeding 50%, previous limb angioplasty, stenting or bypass surgery; or previous limb or foot amputation due to circulatory insufficiency or ankle brachial index of \< 0.9 in at least one limb.), cerebrovascular disease (history of ischemic or hemorrhagic stroke or \> 50% carotid stenosis), or heart failure * Chronic kidney disease with estimated glomerular filtration rate (eGFR) \< 60 ml/min/1.73 m2 or eGFR 60-90 ml/min/1.73 m2 with urine albumin to creatinine ratio (uACR) \> 20 mg/mmol (any previously resolved macroalbuminuria will be considered as a reason for ineligibility, at the investigator's discretion) * Active binge eating disorder or other eating disorder * Uncontrolled mental health disorder * Current use of atypical antipsychotic or corticosteroid * Use of other implanted medical devices, such as pacemakers * Participant whose circumstance is deemed by investigator to be unadvisable, unsafe, or unlikely to be capable of adhering to LCMR and/or isCGM/CBG monitoring during the study period