NCT02846831

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for phase_2

Timeline
Completed

Started Jan 2019

Shorter than P25 for phase_2

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 25, 2016

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 27, 2016

Completed
2.5 years until next milestone

Study Start

First participant enrolled

January 24, 2019

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 27, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 27, 2020

Completed
Last Updated

June 11, 2020

Status Verified

June 1, 2020

Enrollment Period

1 year

First QC Date

July 25, 2016

Last Update Submit

June 8, 2020

Conditions

Keywords

Type 1 diabetesArtificial pancreasClosed-loop systemHypoglycemiaInsulin

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 COMPARATOR

Participants 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.

Other: 12-day intervention with sensor-augmented pump therapyDevice: Insulin pumpDevice: Continuous glucose monitoring systemDrug: Insulin

Single-hormone closed-loop strategy

ACTIVE COMPARATOR

Variable 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.

Other: 12-day intervention with single-hormone closed-loop strategyDevice: Insulin pumpDevice: Continuous glucose monitoring systemDrug: Insulin

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.

Sensor-augmented pump therapy

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.

Single-hormone closed-loop strategy

Tandem Diabetes Care

Sensor-augmented pump therapySingle-hormone closed-loop strategy

Dexcom G5 Platinum

Sensor-augmented pump therapySingle-hormone closed-loop strategy

Participant's usual fast-acting insulin analog will be used: Lispro (Humalog), Aspart (NovoRapid) or Glulisine (Apidra)

Sensor-augmented pump therapySingle-hormone closed-loop strategy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

McGill University Health Centre

Montreal, Quebec, H4A 3J1, Canada

Location

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.

MeSH Terms

Conditions

Diabetes Mellitus, Type 1HypoglycemiaInsulin Resistance

Interventions

MethodsInsulin Infusion SystemsContinuous Glucose MonitoringInsulin

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesAutoimmune DiseasesImmune System DiseasesHyperinsulinism

Intervention Hierarchy (Ancestors)

Investigative TechniquesDrug Delivery SystemsDrug TherapyTherapeuticsInfusion PumpsEquipment and SuppliesArtificial OrgansSurgical EquipmentBlood Chemical AnalysisClinical Chemistry TestsClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisDiagnostic Techniques, EndocrineMonitoring, PhysiologicProinsulinInsulinsPancreatic HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsPeptidesAmino Acids, Peptides, and Proteins

Study Officials

  • Rémi Rabasa-Lhoret

    Institut de recherches cliniques de Montréal

    PRINCIPAL INVESTIGATOR

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

Locations