N/A
Completed N=208
Use of the Guardian™ Connect System With Smart Connected Devices
Source: ClinicalTrials.gov NCT04809285 ↗Enrolled (actual)
208
Serious AEs
2.9%
Results posted
Dec 2024
Primary outcomePrimary: Percentage of Time in Hypoglycemia — 3.1; 2.7 percentage of time
Summary
The purpose of this study is to collect sensor, insulin, sleep, activity and food/meal data for a minimum of 90 days of device wear (Phase 1) and up to a maximum of 9 months of device wear (Phase 2) with optional insulin injection video capture and/or menstrual cycle tracking and/or cardiac monitoring in subjects with insulin requiring diabetes 2-80 years of age.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Time in Hypoglycemia |
3.1; 2.7 | — |
| PRIMARY Percentage of Time in Euglycemia |
59.5; 58.7 | — |
| PRIMARY Percentage of Time in Hyperglycemia |
37.5; 38.7 | — |
Eligibility Criteria
Inclusion Criteria
- Individual is 2-80 years of age at time of consent.
- A clinical diagnosis of type 1 or type 2 diabetes as determined by investigator for:
- at least the last 6 months for subjects 2-6 years of age
- at least the last 12 months for subjects 7-80 years of age
- Subject is on multiple daily injection therapy (3 or more insulin injections per day one of which is a long acting insulin injection), is currently using or is willing and can afford to use insulin pen(s) and pen cartridge(s).
- Subject is currently using or is willing to use the Guardian Connect system during the study.
- Subject agrees to comply with the study protocol requirements.
- For adult subjects: Subject is capable of providing legal consent without a legal authorized representative.
Exclusion Criteria
- Subject is using a syringe and unwilling or unable to use insulin pen(s).
- Subject is using an insulin pump.
- Subject is currently using a non-Medtronic standalone CGM system and unwilling to use only the Guardian Connect system during the study.
- Subject is using hydroxyurea at time of screening or plans to use it during the study.
- Subject will not tolerate tape adhesive in the area of device placement as assessed by a qualified provider.
- Subject has any unresolved adverse skin condition in the area of device placement (e.g. psoriasis, rash, Staphylococcus infection).
- Subject is actively participating in or plans to enroll in an investigational study (e.g. drug or device), other than this study, wherein they have received treatment from an investigational drug or device.
- Subject has a positive urine pregnancy test at time of screening.
- Subject is female, sexually active without the use of contraception, able to become pregnant or plans to become pregnant during the course of the study.
- Subject is unwilling to participate in study procedures.
- Subject is directly involved in the study as research staff.
Data sourced from ClinicalTrials.gov (NCT04809285). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.