A Research Study in Italy to Understand How the Dose Check App Used With Xultophy® Treatment Helps to Control Blood Sugar Level
Study Details
Study Description
Brief Summary
This will study look at how a mobile based app called 'Dose Check' used along with Xultophy® helps to control blood sugar level in participants with type 2 diabetes mellitus (T2DM). Participants will get Xultophy® as prescribed by study doctor or will continue already prescribed treatment with Xultophy®. Participants will also be prescribed to use Dose Check app by study doctor. Participants will be asked to install the Dose Check app in their mobile phone, which will support with the correct dose of Xultophy®. The study will last for about 6 to 7 months.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| IDegLira + Dose Check Participants will be treated with commercially available IDegLira used with Dose Check app according to local label and routine clinical practice at the discretion of the treating physician. |
Drug: IDegLira
Pre-filled pen injection.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Change in glycated haemoglobin (HbA1c) [From baseline (week 0) to end of the study (EOS) visit (week 26)]
Measured in Percentage point.
Secondary Outcome Measures
- Participants reaching individual HbA1c target set by physician [At EOS visit (week 26)]
Measured as count of participants (yes/no).
- Participants reaching physician set individual fasting blood glucose (FBG) target [From baseline (week 0) to EOS visit (week 26)]
Measured as count of participants (yes/no).
- Time to physician set individual FBG target from first reported FBG [From baseline (week 0) to EOS visit (week 26)]
Measured in number of weeks.
- Participants achieving target level FBG according to clinical guidance [From baseline (week 0) to EOS visit (week 26)]
Measured as count of participants (yes/no).
- Change in laboratory measured FPG [From baseline (week 0) to EOS visit (week 26)]
Measured in milligrams per deciliter (mg/dL).
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Signed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol).
-
Male or female, age above or equal to 21 years at the time of signing informed consent.
-
Diagnosed with T2DM >=12 weeks prior to signing consent.
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The decision to initiate treatment with commercially available Dose Check app as a part of treatment along with Xultophy® as per the local label has been made by the patient and the treating physician before and independently from the decision to include the participant in this study.
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Participants who are insulin naïve (an exception is short-term insulin treatment for acute illness for a total of less than (<) 14 days) or already on treatment with Xultophy® at Visit 1 for less than or equal to (<=) 3 months and <=15 dose steps.
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Available HbA1c value <=12 weeks prior to the 'Informed consent and initiation of Dose Check app visit' (V1) or HbA1c measurement taken in relation with the 'Informed consent and initiation of Dose Check app visit' (V1), if in line with local clinical practice.
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Willingness to continue using the Dose Check app on a compatible smartphone according to the intended use for the entire duration of the study.
Exclusion Criteria:
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Previous participation in this study. Participation is defined as having signed informed consent in this study.
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Women known to be pregnant or breastfeeding, or women planning to become pregnant during the conduct of the study.
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Treatment with any investigational drug or Software as Medical Device (SaMD) within 30 days prior to enrolment into the study.
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Diagnosed with type 1 diabetes mellitus.
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Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.
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Hypersensitivity to the active substance or any of the excipients as specified in the Xultophy® local label.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Novo Nordisk Investigational Site | Catanzaro | Cz | Italy | 88100 |
| 2 | Novo Nordisk Investigational Site | Catania | Italy | 95126 |
Sponsors and Collaborators
- Novo Nordisk A/S
Investigators
- Study Director: Clinical Transparency (dept. 2834), Novo Nordisk A/S
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- NN9068-7589
- U1111-1288-8131