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InPenTM User Experience

InPenTM User Experience - InPenTM User Experience

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51113
Enrollment
20
Registered
2021-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 diabetes

Interventions

Run-In Period: 2 weeks Visit 1 (Office): Consent only Visit 2 (Office): Screening/Baseline (including baseline demographics and HbA1c) and Start Run-In o Eligibility has been confirmed (Visit 1 and

Sponsors

Medtronic Trading NL BV
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1.Subject is aged 18-75 years at time of screening 2.Subject is on MDI therapy (defined as * 3 insulin injections per day and on a basal/bolus regimen) *1 year prior to screening 3.Subject has a clinical diagnosis of type 1 diabetes for 1 year prior to screening 4.Subject has a Glycosylated hemoglobin (HbA1c) less than 10% as assessed by local lab

Exclusion criteria

Exclusion criteria: 1. Women of child-bearing potential who have a positive pregnancy test at screening or plan to become pregnant during the course of the study. 2. Women who are breastfeeding. 3. Subject has any unresolved adverse skin conditions in the area of sensor placement (e.g. psoriasis, dermatitis herpetiformis, rash, Staphylococcus infection). 4. Subject is actively participating in an investigational study (drug or device) wherein he/she has received treatment from an investigational study drug or device in the last 2 weeks before enrollment into this study, as per investigator judgment. 5. Subject is currently abusing illicit drugs, marijuana, alcohol or prescription drugs (other than nicotine), per investigator judgment. 6. Subject has any other disease or condition that may preclude the patient from participating in the study, per investigator judgment. 7. Subject is legally incompetent, illiterate or vulnerable person. 8. Research staff involved with executing the study.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)