Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 2020) in Adult Subjects With Type 1 Diabetes (CIP347)

Launched by MEDTRONIC DIABETES · Dec 13, 2024

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ClinConnect Summary

This clinical trial is studying a new device called the Medtronic Implantable Insulin Pump System (MIIPS 2020) for adults with Type 1 diabetes. The goal is to see how well this device works for people whose diabetes is hard to control with regular insulin shots or external insulin pumps, especially those who experience serious highs or lows in blood sugar levels without clear reasons. If you're an adult aged 18 or older and have been diagnosed with Type 1 diabetes for at least six months, you might be eligible to participate, especially if you’re struggling with blood sugar management despite current treatments.

Participants in the trial will have the chance to use this new implantable system, which is designed to help regulate insulin delivery more effectively. You will need to be able to operate the device and monitor your glucose levels regularly. It's important to have a reliable support person, like a family member or friend, who can help you in case of emergencies. The trial is currently looking for volunteers, and if you're considering joining, you'll be provided with detailed information and support throughout the study to ensure your safety and well-being.

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Eligibility criteria

• Inclusion Criteria:
• • 1. Subject is aged ≥ 18 years old.
• • 2. Subject has a clinical diagnosis of type 1 diabetes for ≥ 6 months prior to screening as determined via medical record or source documentation by an individual qualified to make a medical diagnosis.
• • 3. Subject with type 1 diabetes mellitus that cannot be controlled with subcutaneous insulin therapy (including external pump), presenting with frequent, otherwise unexplained severe hyper-and/or hypoglycaemia.
• • 4. Subject has access to a reliable support person, defined as an individual who has daily contact with the subject and knows who to contact in the event of an emergency (i.e., caregiver).
• • 5. Subject has the physical and intellectual ability (in the opinion of the study investigator) to operate the MIIP system and to comply with the data reporting requirements of the study.
• • 6. Subject is willing and able to sign and date informed consent, comply with all study procedures as required during the study.
• Exclusion Criteria:
• • 1. Subject is actively participating in an investigational study (drug or device) wherein he/she has received treatment from an investigational study drug or device before enrollment into this study, that could impact the outcomes of this study; as per investigator and sponsor judgment.
• • 2. Subject has any other disease or condition that may increase risks during the implant procedure or may preclude the subject from participating in the study, as determined by a physician who is not the principal investigator.
• • 3. Subject has any known or suspected allergy to insulin or implantable materials of the MIIPS (pump and catheter) as determined by a physician.
• • 4. Subject is a woman who is pregnant, of childbearing potential or lactating, and who is neither surgically sterile nor using contraceptives (devices, oral, implanted or other physician-approved contraceptive) at the time of enrollment.
• • 5. Subject is vulnerable, legally incompetent or illiterate.
• • 6. Residence or planned non-pressurized travel at elevations above 10000 feet/3048 meters (commercial airline travel is acceptable).
• • 7. Planning to engage in activities requiring a descent greater than or equal to 10 feet/3 meters below sea level.
• • 8. Subject has an active infection requiring antibiotic treatment.
• • 9. Subject is a person whose body size is not sufficient to accept implantable pump bulk and weight.
• • 10. Subject has a life expectancy of less than 9 months.
• • 11. Subject has diagnosis of illicit drugs abuse disorder.
• • 12. Subject has diagnosis of marijuana abuse disorder.
• • 13. Subject has diagnosis of prescription drugs abuse disorder.
• • 14. Subject has diagnosis of alcohol abuse disorder.
• • 15. Subject who is unwilling or unable to monitor their glucose level or wear a personal continuous glucose monitor.
• • 16. Subject who is unwilling or unable to make programming modifications to the pump based on glucose level readings.