The Steno 780G Study
Study Details
Study Description
Brief Summary
Treatment with insulin pumps and sensor-based glucose monitoring has proven superior to other treatment methods in type 1 diabetes. Still, the majority of people treated with insulin pumps and glucose sensors still does not meet the recommended sensor-based glycaemic targets. Automated insulin delivery systems, also known as closed-loop systems, have shown to improve TIR, TAR, and TBR compared with insulin pump and CGM systems that cannot automatically dose insulin.
The primary objective of the Steno 780G study is to test the effects of the MiniMed 780G system in persons with T1D treated with insulin pump and CGM/isCGM who are not meeting glycaemic targets.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: 780G-780G Participants will use MiniMed 780G system for 14 weeks + 14 weeks |
Device: Minimed 780G insulin pump
This will be a 14-week, open-label, randomised, parallel-group, controlled trial comparing the efficacy of an AHCL system (MiniMed 780G, Medtronic Diabetes, Northridge, CA) with usual care (i.e., a person's usual insulin pump and CGM/isCGM system). After the 14-week trial period, the control group switches to treatment with the MiniMed 780G system. The intervention group continues with the MiniMed 780G system. Both groups are monitored for another 14 weeks.
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| Placebo Comparator: Usual Care - 780G Participants will continue with their usual insulin pump for 14 weeks. After completion of the first 14-week periode, they switch to 780G for another 14 weeks. |
Device: Minimed 780G insulin pump
This will be a 14-week, open-label, randomised, parallel-group, controlled trial comparing the efficacy of an AHCL system (MiniMed 780G, Medtronic Diabetes, Northridge, CA) with usual care (i.e., a person's usual insulin pump and CGM/isCGM system). After the 14-week trial period, the control group switches to treatment with the MiniMed 780G system. The intervention group continues with the MiniMed 780G system. Both groups are monitored for another 14 weeks.
|
Outcome Measures
Primary Outcome Measures
- Difference between treatment groups in change in TIR (3.9-10.0 mmol/l) from baseline to Week 14 [From baseline to week 14]
Difference between treatment groups in change in TIR (3.9-10.0 mmol/l) from baseline to Week 14 assessed by 2 weeks of CGM data (12 AM-12 AM (wake + sleep)).
Secondary Outcome Measures
- Difference between treatment groups in change in TIR (3.9-10.0 mmol/l) from baseline to Week 14 assessed by 2-week CGM data (6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep)) [From baseline to week 14]
- Difference in mean glucose [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep)):
- Difference in standard deviation [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep)):
- Difference in coefficient of variation [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep)):
- Percentage of time with glucose values < 3.9 mmol/l (TBR level 1). [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep)):
- Percentage of time with glucose values < 3.0 mmol/l (TBR level 2). [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep)):
- Percentage of time with glucose values > 10.0 mmol/l (TAR level 1). [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to
- Percentage of time with glucose values > 13.9 mmol/l (TAR level 2). [From baseline to week 14]
difference in change in the given variable between treatment groups from baseline to Week 14 assessed by 2 weeks of CGM data (each of the endpoints will be calculated for the following 3-time intervals: 6 AM - 12 AM (wake), and 12 AM - 6 AM (sleep), 12 AM - 12AM (wake + sleep))
- Glucose management indicator (an estimate of the laboratory HbA1c value). [From baseline to week 14]
From insulin pump data downloads
- HbA1c [From baseline to week 14]
- Body weight [From baseline to week 14]
- Total daily insulin dose [From baseline to week 14]
Total daily insulin dose assessed by 2-week insulin pump data downloads
- Total daily carbohydrate intake [From baseline to week 14]
Total daily carbohydrate intake assessed by 2-week insulin pump data downloads.
Other Outcome Measures
- Number of daily carbohydrate entries in the insulin pump assessed by 2-week insulin pump data downloads [From baseline to week 14]
assessed by 2-week insulin pump data downloads
- Hypoglycaemia awareness status. [From baseline to week 14]
Assesed by GOLD and Pedersen-Bjerggaard scale, low scores means aware, high scores means unawareness
- Diabetes Treatment Satisfaction Questionnaire scores [From baseline to week 14]
Assessed by Diabetes Treatment Satisfaction Questionnaire. Scores from -36 to 36, high scores means higher satisfaction
- Hypoglycaemia Fear Survey scores [From baseline to week 14]
Assessed by Hypoglycemia Fear Survey questionnaire. Scores from 0 to 52, higher scores indicate worse outcome
- Diabetes Distress Scale scores [From baseline to week 14]
Assessed by Diabetes Distress Scale questionnaire. DDS consists of 17 items on a 6-point scale. A score of ≥3 indicates a high diabetes distress and a score lower than 3 and ≥2 indicates a moderate diabetes distress.
- Pittsburgh Sleep Quality Index scores [From baseline to week 14]
Assessed by PTQI questionnaire
- Sleep efficiency (%) assessed by Actigraph GT3x [From baseline to week 14]
assessed by Actigraph GT3x
- Physical activity level (sedentary, light, moderate-to-vigorous) assessed by Actigraph GT3x [From baseline to week 14]
assessed by Actigraph GT3x
- Difference in number of severe hypoglycaemia events (cognitive impairment requiring external assistance for recovery). [From baseline to week 14]
Assessed by questionnaire
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age 18-75 years
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Type 1 diabetes ≥2 years.
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HbA1c >=58 mmol/mol
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Insulin pump treatment ≥12 months
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CGM or isCGM use ≥6 months
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Novorapid use ≥4 weeks
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Carbohydrate counting and use of the insulin pump bolus calculator for most snacks and meals.
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Carbohydrate intake >80 grams per day (assessed by review of intake recorded in the insulin pump during the 2 weeks prior to the screening visit)
Exclusion Criteria:
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Breast-feeding, pregnancy or planning to become pregnant.
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Use of anti-diabetic medicine (other than insulin), corticosteroids or other drugs affecting glucose metabolism during the study period or within 30 days prior to study start.
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Use of hybrid closed-loop systems
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Daily use of paracetamol (acetaminophen)
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Alcohol or drug abuse.
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Severe cardiac disease or retinopathy contraindicating HbA1c <53 mmol/mol.
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Other concomitant medical or psychological condition that according to the investigator's assessment makes the person unsuitable for study participation.
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Lack of compliance with key study procedures at the discretion of the investigator.
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Unacceptable adverse events at the discretion of the investigator.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Steno Diabetes Center Copenhagen | Gentofte | Denmark | 2820 |
Sponsors and Collaborators
- Steno Diabetes Center Copenhagen
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Steno 780G