Clinical Study to Evaluate the Impact of the Accu-Chek SmartGuide CGM Solution on the Mean Change in Time in Range Compared With Self-Monitoring of Blood Glucose in Participants With Type 1 and Type 2 Diabetes Mellitus
About this study
This is an open label, two-arm, randomized multi-center clinical device study in adult subjects with Type 1 diabetes (T1D) or insulin-dependent Type 2 diabetes (T2D) on a multiple daily injection (MDI) regime. The goal of the study is to investigate the impact of the Accu-Chek SmartGuide CGM solution on the change in overall time in range (TIR) of blood glucose concentrations of 70-180 mg/dl compared with that using self-monitoring of blood glucose (SMBG).
- Condition
- Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus
- Tested
- Accu-Chek SmartGuide CGM Solution, Accu-Chek SmartGuide Sensor and Blinded Apps, SMBG Device
- Sponsor
- Hoffmann-La Roche
Who can join
- Age
- 18 years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
Inclusion 5
- Minimum age: 18 years
- Study condition: Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus
- Type 1 Diabetes mellitus (T1D) or Type 2 Diabetes mellitus (T2D) diagnosed at least 12 months prior to screening, using multiple daily injection (MDI) regime for at least six months prior to screening
- Performing SMBG, no CGM/flash glucose monitoring (FGM) use during the last six months prior screening
- HbA1c ≥8% and ≤10% based on analysis from a local laboratory
Exclusion 23
- Untreated adrenal or thyroid insufficiency
- Severe visual impairment
- Significant renal impairment: eGFR \<30 ml/min within last one year
- Serious acute or chronic concomitant disease or an anamnesis which might, in the opinion of the investigator, pose a risk to the subject
- Hematocrit greater than 10% below the lower limit of normal
- Pregnancy (lack of negative pregnancy test - except in case of menopause, sterilization or hysterectomy - self-reported), planned pregnancy, or breast feeding
- Allergic to the adhesive (glue or tape)
- Skin diseases (e.g. psoriasis vulgaris, bacterial skin diseases) at the sensor application sites
- Sickle cell disease, or hemoglobinopathy
- Elective surgery planned that requires general anesthesia during study participation
- Current or anticipated acute uses of glucocorticoids (oral, injectable, or intravenous)
- Medical conditions that, per investigator determination, make it inappropriate or unsafe to target an HbA1c of \<7%.
- Conditions may include but are not limited to: heart failure, unstable cardiovascular disease, recent myocardial infarction, ventricular rhythm disturbances, recent transient ischemic attack or cerebrovascular accident, significant malignancy
- Chronic use of opiates, opioids, morphinomimetics more than three times per week, which has not stopped at least 30 days prior to screening and any other medication interfering with the assessment of pain, as per investigator's discretion
- Intake of hydroxyurea (hydroxycarbamide), levodopa, methyldopa, ascorbic acid, acetylsalicylic acid (≥300mg), which has not stopped at least 30 days prior to screening
- Magnetic resonance tomography (MRT), computed tomography (CT), X-ray, radiofrequency ablation, high-frequency electrical heat or high intensity focused ultrasound planned during the course of the study
- Planned flight or high-altitude hike (\>3000 m) during baseline and assessment periods
- Shift-worker (night-shifts)
- On or planning to start a diet intended for weight change
- Currently abusing illicit and/or prescription drugs or alcohol as judged by the investigator
- Any other physical or psychological disease or psychiatric disorder that could limit adherence to the required study tasks and interfere with the normal conduct of the study as judged by the investigator
- Dependency (e.g., employee, co-worker or family member) on sponsor, investigator or companies active in the field of CGM (e.g. Dexcom, Abbott, Menarini, Medtronic) or their subsidiaries
- Participation in another clinical study at the same time
Where
19 sites, 19 recruiting
Centrum Badań Klinicznych PI-House sp. z o.o.
Gdansk, Poland
Diabetes Technology Center, Jagiellonian University Medical College
Krakow, Poland
NZOZ Neuromed
Kraśnik, Poland
NZOZ Neuromed
Lublin, Poland
Institute of Rural Health
Lublin, Poland
KO-MED Centra Kliniczne Lublin II
Lublin, Poland
and 13 more sites on ClinicalTrials.gov
Contact
-
Study ID Reference: DC000129 Roche Diabetes Care Poland and Turkey
+48 22 481 55 00; 08002113636 polska.diabetologia@roche.com; diyabetevi.turkey@roche.com
Potential match only. Final eligibility is determined by the study team.