Closed-loop Control of Glucose Levels (Artificial Pancreas) for 12 Days in Adults With Type 1 Diabetes
An Open-label, Randomized, Two-way, Cross-over Study to Assess the Efficacy of Single-hormone Closed-loop Strategy and Sensor-augmented Pump Therapy in Regulating Glucose Levels for 12 Days in Free-living Outpatient Conditions in Patients With Type 1 Diabetes
1 other identifier
interventional
36
1 country
2
Brief Summary
Closed-loop strategy is composed of three components: glucose sensor to read glucose levels, insulin pump to infuse insulin and a dosing mathematical algorithm to decide on the required insulin dosages based on the sensor's readings. The objective of this study is to compare the effectiveness of single-hormone closed-loop and sensor-augmented pump therapy in regulating day-and-night glucose levels in adults with T1D for 12 days in outpatient settings. The investigators hypothesize that dual-hormone closed-loop will increase the percentage of time of glucose levels spent in the target range in adults compared to single-hormone closed-loop, which in turn will be more effective than sensor-augmented pump therapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Jan 2019
Shorter than P25 for phase_2
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 25, 2016
CompletedFirst Posted
Study publicly available on registry
July 27, 2016
CompletedStudy Start
First participant enrolled
January 24, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 27, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
January 27, 2020
CompletedJune 11, 2020
June 1, 2020
1 year
July 25, 2016
June 8, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Percentage of time of glucose levels spent between 3.9 and 10 mmol/L.
288 hours
Secondary Outcomes (37)
Percentage of time of glucose levels spent between 3.9 and 7.8 mmol/L
288 hours
Percentage of time of glucose levels spent below 3.9 mmol/L
288 hours
Percentage of time of glucose levels spent below 3.3 mmol/L
288 hours
Percentage of time of glucose levels spent below 2.8 mmol/L
288 hours
Percentage of time of glucose levels spent above 10.0 mmol/L
288 hours
- +32 more secondary outcomes
Study Arms (2)
Sensor-augmented pump therapy
ACTIVE COMPARATORParticipants will use sensor-augmented pump therapy with low-glucose suspend to regulate glucose levels. The low-glucose suspend feature available in the MiniMed® Paradigm® Veo™, Medtronic combined with the Enlite sensor® will be used. This feature allows for suspension of insulin delivery at a pre-set sensor glucose value for up to 2 hours.
Single-hormone closed-loop strategy
ACTIVE COMPARATORVariable subcutaneous insulin infusion will be used to regulate glucose levels. Participant's usual fast-acting insulin analog will be infused using a subcutaneous infusion pump (MiniMed® Paradigm® Veo™, Medtronic). Every 10 minutes, the glucose levels as measured by the sensor (Enlite sensor®, Medtronic) will be transferred automatically to a smartphone, that harbors the algorithm, that will calculate the recommended doses and will send it wirelessly to the infusion pump.
Interventions
A sensor will be inserted on the day before the start of the intervention by the participants. The participant will also have to install the study insulin pump. Participants will be advised to continue with study intervention at home for the next 12 days. Participants will have been previously shown how to use the study insulin pump.
A sensor will be inserted on the day before the start of the intervention by the participants. On the first day of the intervention, participants will be admitted to the clinical research facility anytime between 8:00 am and 11:30 am. Training on connection and disconnection of the system, meal boluses, etc. will be given. Only participants demonstrating competency on use of study devices will be allowed to continue to the home study phase. Participants will be advised to continue with study intervention at home for the next 12 days.
Tandem Diabetes Care
Dexcom G5 Platinum
Participant's usual fast-acting insulin analog will be used: Lispro (Humalog), Aspart (NovoRapid) or Glulisine (Apidra)
Eligibility Criteria
You may qualify if:
- Males and females ≥ 18 years of old.
- Clinical diagnosis of type 1 diabetes for at least one year.
- The subject will have been on insulin pump therapy for at least 3 months.
- HbA1c ≤ 12%.
You may not qualify if:
- Clinically significant nephropathy, neuropathy or retinopathy as judged by the investigator
- Recent (\< 6 months) acute macrovascular event e.g. acute coronary syndrome or cardiac surgery
- Warfarin chronic treatment if INR monitoring cannot be evaluated (can increase the risk of bleeding)
- Chronic use of acetaminophen. Acetaminophen may interfere with glucose sensor readings
- Pregnancy (ongoing or current attempt to become pregnant)
- Breastfeeding
- No nearby party for assistance if needed
- Plans to go abroad or travel at more than 2 hours distance from Montreal during the trial period
- Severe hypoglycemic episode within two weeks of screening or during the run-in period
- Severe hyperglycemic episode requiring hospitalization in the last 3 months
- Current use of glucocorticoid medication (except low stable dose and inhaled steroids)
- Known or suspected allergy to the trial products
- Other serious medical illness likely to interfere with study participation or with the ability to complete the trial by the judgment of the investigator
- Anticipation of a significant change in exercise regimen between admission and end of the trial (i.e. starting or stopping an organized sport)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Institut de recherches cliniques de Montréal
Montreal, Quebec, H2W 1R7, Canada
McGill University Health Centre
Montreal, Quebec, H4A 3J1, Canada
Related Publications (1)
Haidar A, Legault L, Raffray M, Gouchie-Provencher N, Jacobs PG, El-Fathi A, Rutkowski J, Messier V, Rabasa-Lhoret R. Comparison Between Closed-Loop Insulin Delivery System (the Artificial Pancreas) and Sensor-Augmented Pump Therapy: A Randomized-Controlled Crossover Trial. Diabetes Technol Ther. 2021 Mar;23(3):168-174. doi: 10.1089/dia.2020.0365. Epub 2020 Dec 31.
PMID: 33050728DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rémi Rabasa-Lhoret
Institut de recherches cliniques de Montréal
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Medicine
Study Record Dates
First Submitted
July 25, 2016
First Posted
July 27, 2016
Study Start
January 24, 2019
Primary Completion
January 27, 2020
Study Completion
January 27, 2020
Last Updated
June 11, 2020
Record last verified: 2020-06