Evaluation of Medtronic DUO Extended Set

Early Feasibility Study: Evaluation of Medtronic Duo Extended Set With 670G Pump Therapy

This study is a single-center, non-randomized, prospective single arm study of adult subjects with type 1 diabetes utilizing 670G insulin pump therapy with Continuous Glucose Monitoring (CGM). These subjects will be using 4 DUO Extended sets that will serve as an exploratory pilot study to assess the 7-day survival of the Duo Extended set.

Study Overview

• Status: Recruiting
• Conditions: Diabetes Mellitus, Type 1
• Intervention / Treatment: Device: Experimental prospective single arm evaluating the Medtronic Duo Extended Set

Detailed Description

Up to 20 adult subjects will be enrolled at the research center. Atlanta Diabetes Associates (ADA), with at least 15 subjects meeting the eligibility criteria. Eligibility criteria will be assessed at the screening visit and confirmed prior to Visit 2. At Visit 2, subjects will be provided supplies, including the DUO device, and will be trained on insertion. Each subject will wear their own MiniMed 670G insulin system including Guardian sensor (new sensor with transmitter will be provided for the study) and a DUO Extended set. The infusion set in the DUO Extended will be used for insulin infusion and the sensor in the DUO Extended will be blinded with a specific recorder connected to each sensor.

Guardian Sensor (3) and the SMBG measurements will be used for making therapy decisions as approved for the 670G system. Subjects will upload their pump, Contour meter and GS3 sensor data each week, which will be reviewed by an investigator. Subjects will wear the DUO device for a total of four weeks. At Visit 6, subjects will come to the site to have devices uploaded, to return the investigational devices, to have a skin assessment and for labs to be drawn.

• Study Type: Interventional
• Enrollment (Anticipated): 20
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Melody L Cantrell, PharmD; Phone Number: 850 404-355-4393; Email: mcantrell@atlantadiabetes.com
• Study Contact Backup: Name: Betsy Childs, RN; Phone Number: 404-355-4393; Email: bchilds@atlantadiabetes.com

Study Locations

• United States
  • Georgia
    • Atlanta, Georgia, United States, 30318
      • Recruiting
      • Atlanta Diabetes Associates
      • Contact: Melody L Cantrell, PharmD; Phone Number: 850 404-355-4393; Email: mcantrell@atlantadiabetes.com
      • Contact: Betsy Childs, RN; Phone Number: 404-355-4393; Email: bchilds@atlantadiabetes.com
      • Principal Investigator: Bruce W Bode, MD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Has type 1 diabetes for more than one year.
2. Subject is on the MiniMed 670G insulin pump therapy within1 year prior to screening.
3. Subject is currently using Auto Mode at least 75% of the time and willing to utilize Auto Mode and Duo device during the study.
4. Subject is willing and able to perform study procedures as per investigator discretion.
5. Subject is willing to take one of the following two insulins: Humalog or Novolog

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 investigational study device in the last 2 weeks.
2. Subject is female and has a positive pregnancy screening test.
3. Subject is female of childbearing age and who is sexually active should be excluded if she is not using a form of contraception deemed reliable by investigator.
4. Subject is female and plans to become pregnant during the study.
5. Subject has Glycosylated hemoglobin (HbA1c) > 8.5 % at time of screening.
6. Subject has had a history of 1 or more episodes of severe hypoglycemia.
7. Subject has taken any oral, injectable, or IV glucocorticoids within 8 weeks from time of screening visit, or plans to take any oral, injectable, or IV glucocorticoids during the course of the study.
8. Subject is unable to tolerate tape adhesive in the area of Duo™ Extended set or sensor.
9. Subject has any unresolved adverse skin condition, including infection, in the area of Duo™ Extended set or sensor placement (e.g., psoriasis, dermatitis herpetiformis, rash, Staphylococcus infection).
10. Subject has had Diabetic Ketoacidosis (DKA) in the 12 months prior to screening visit.
11. Subject is currently abusing illicit drugs.
12. Subject is currently abusing alcohol.
13. Subject has history of adrenal disorder.
14. Subject has a history of inpatient psychiatric treatment in the past 6 months prior to screening.
15. Subject has any condition that the Investigator believes would interfere with study participation.
16. Subject has a history of visual impairment which would not allow subject to participate in the study and perform all study procedures safely, as determined by the investigator.
17. Subject has a sickle cell disease, hemoglobinopathy; or has received red blood cell transfusion or erythropoietin within 3 months prior to time of screening.
18. Subject plans to receive red blood cell transfusion or erythropoietin over the course of study participation.
19. Subject is using pramlintide (Symlin), SGLT2 inhibitors, GLP agonists, biguanides, DPP-4 inhibitors or sulfonylureas more than 2 weeks from time of screening.
20. Subject has been diagnosed with chronic kidney disease, having an estimated glomerular filtration rate (eGFR)< 60mL/min/1.73 m2, requiring dialysis, or resulting in chronic anemia.
21. Subject has history of cardiovascular disease defined as any ischemic related event or clinically significant arrythmia.
22. Subject has hypothyroidism and has out of reference range thyroid-stimulating hormone (TSH) on screening visit.
23. Subject plans to have medical imagining (e.g., MRI, diathermy services, CT scans, etc.) over the course of the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Medtronic Duo Extended Set; These subjects will be using 4 Duo Extended sets that will serve as an exploratory pilot study to assess the 7-day survival of the Duo Extended set.	Device: Experimental prospective single arm evaluating the Medtronic Duo Extended Set; Subjects will be using 4 Duo extended sets that will serve as an exploratory pilot study to assess the 7-day survival of the Duo Extended set.; Other Names: Medtronic DUO Extended Set with 670G Pump Therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of subjects with Duo Extended set failures due to unexplained hyperglycemia (i.e. suspected occlusion) at the end of Day 7.	Unexplained hyperglycemia	7 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of subjects with a rate of infusion set survival of 7 days or greater, excluding those that kinked on insertion or accidentally pulled out.	Infusion set survival	7 days

Collaborators and Investigators

• Sponsor: Atlanta Diabetes Associates
• Collaborators: Medtronic
• Investigators: Principal Investigator: Bruce W Bode, MD, Atlanta Diabetes Associates

Study record dates

Study Major Dates

• Study Start (Actual): March 18, 2021
• Primary Completion (Anticipated): October 1, 2021
• Study Completion (Anticipated): November 1, 2021

Study Registration Dates

• First Submitted: March 18, 2021
• First Submitted That Met QC Criteria: March 29, 2021
• First Posted (Actual): March 30, 2021

Study Record Updates

• Last Update Posted (Actual): March 30, 2021
• Last Update Submitted That Met QC Criteria: March 29, 2021
• Last Verified: March 1, 2021

More Information

Terms related to this study

• Keywords: Diabetes Type 1
• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Immune System Diseases; Autoimmune Diseases; Endocrine System Diseases; Diabetes Mellitus; Diabetes Mellitus, Type 1
• Other Study ID Numbers: ADA-001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes