Closed-loop Control of Overnight Glucose Levels in Adults and Adolescents With Type 1 Diabetes
18 oktober 2014 uppdaterad av: Rémi Rabasa-Lhoret, Institut de Recherches Cliniques de Montreal
An Open-label, Randomized, Three-way, Multicenter Study to Compare the Efficacy of Single-hormone Closed-loop Strategy, Dual-hormone Closed-loop Strategy and Conventional Insulin Pump Therapy in Regulating Overnight Glucose Levels at Home in Adolescents and Adults With Type 1 Diabetes
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. A dual-hormone closed-loop system would regulate glucose levels through the infusion of two hormone: insulin and glucagon.
The main objective of this project is to compare the efficacy of single-hormone closed-loop strategy, dual-hormone closed-loop strategy and pump therapy to regulate overnight glucose levels in a out-patient study in adults and adolescents with type 1 diabetes.
The investigators hypothesized that dual-hormone closed-loop strategy is more effective in regulating overnight glucose levels in adults and adolescents with type 1 diabetes compared to single-hormone closed-loop strategy, which in turn is more effective than the conventional pump therapy.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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. A dual-hormone closed-loop system would regulate glucose levels through the infusion of two hormone: insulin and glucagon.
We aim to conduct a multicenter study to compare the efficacy of conventional pump therapy, single-hormone closed-loop strategy and dual-hormone closed-loop strategy to regulate overnight glucose levels, at home, in adolescents and adults with type 1 diabetes. Each intervention will be tested on two nights: 1) After a carbohydrate-rich dinner meal (to exaggerate hyperglycemic risk and; 2) After an evening exercise (to exaggerate hypoglycemic risk).
Studietyp
Interventionell
Inskrivning (Faktisk)
28
Fas
- Fas 2
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Ontario
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Toronto, Ontario, Kanada
- Mount Sinai Hospital
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Quebec
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Montreal, Quebec, Kanada
- Institut de recherches cliniques de Montréal
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Montreal, Quebec, Kanada
- Montreal Children Hospital
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-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
12 år och äldre (Barn, Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Males and females aged ≥ 12 years of old.
- Body mass index < 35
- Clinical diagnosis of type 1 diabetes for at least one year.
- The subject will have been on insulin pump therapy for at least 4 months.
- HbA1c < 12%.
- At least two visits with an endocrinology team in the past 1 year.
Exclusion Criteria:
- Clinically significant nephropathy, neuropathy (peripheral or autonomic e.g. significant gastroparesis) or retinopathy as judged by the investigator.
- Recent (< 6 months) acute macrovascular event e.g. acute coronary syndrome or cardiac surgery.
- A recent injury to body or limb, muscular disorder, use of any medication or other significant medical disorder if that injury, medication or disease in the judgment of the investigator will affect the completion of the exercise protocol.
- Ongoing pregnancy.
- Severe hypoglycemic episode within two weeks of screening.
- Current use of glucocorticoid medication (except low stable dose and inhaled therapy).
- Known or suspected allergy to the insulin aspart, glucagon, Medtronic sensors, or Medtronic infusion sets..
- Other serious medical illness likely to interfere with study participation or with the ability to complete the trial by the judgment of the investigator.
- Anticipating a significant change in treatment regimen between admissions (such as a major change in an exercise routine, significant change in dietary routine or in insulin therapy.
- Failure to comply with team's recommendations.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Crossover tilldelning
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Conventional insulin pump therapry
Subjects will use conventional pump therapy to regulate their glucose levels.
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At 19:30, patients will eat a standardized large meal (110g carbohydrate for males; 90g carbohydrate for females).
Conventional insulin pump therapy or closed-loop system will be use to control glucose levels from 21:00 until 7:00 next morning.
Study participants will go to a training facility around 18:00 to perform a 60min workout at 60% heart rate reserve.
The workout will be on a treadmill and/or a stationary bicycle.
Conventional insulin pump therapy or closed-loop system will be use to regulate glucose levels from 21:00 until 7:00 next morning.
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|
Aktiv komparator: Single-hormone closed-loop system
Variable subcutaneous insulin infusion rate will be used to regulate glucose levels.
Insulin Aspart (Novorapid) will be infused using a subcutaneous infusion pump.
The glucose level as measured by the real time sensor will be entered manually into the computer every 10 minutes.
The pump's infusion rate will then be changed manually based on the computer-generated recommendations of infusion rates.
|
At 19:30, patients will eat a standardized large meal (110g carbohydrate for males; 90g carbohydrate for females).
Conventional insulin pump therapy or closed-loop system will be use to control glucose levels from 21:00 until 7:00 next morning.
Study participants will go to a training facility around 18:00 to perform a 60min workout at 60% heart rate reserve.
The workout will be on a treadmill and/or a stationary bicycle.
Conventional insulin pump therapy or closed-loop system will be use to regulate glucose levels from 21:00 until 7:00 next morning.
|
|
Aktiv komparator: Dual-hormone closed-loop system
Insulin Aspart (Novorapid) and glucagon (Paladin) will be infused using two separate subcutaneous infusion pumps.
The glucose levels as measured by the real time sensor will be entered manually into the computer every 10 minutes.
The pumps' infusion rate will then be changed manually based on the computer generated-recommendation delivery levels.
|
At 19:30, patients will eat a standardized large meal (110g carbohydrate for males; 90g carbohydrate for females).
Conventional insulin pump therapy or closed-loop system will be use to control glucose levels from 21:00 until 7:00 next morning.
Study participants will go to a training facility around 18:00 to perform a 60min workout at 60% heart rate reserve.
The workout will be on a treadmill and/or a stationary bicycle.
Conventional insulin pump therapy or closed-loop system will be use to regulate glucose levels from 21:00 until 7:00 next morning.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Percentage of time in target range
Tidsram: 8 hours
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Percentage of time for which glucose levels (as measured by the glucose sensor) are in target range.
Target range is defined to be between 4.0 to 8.0 mmol/L
|
8 hours
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Percentage of time in target range for each night separately
Tidsram: 8 hours
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Percentage of time for which glucose levels are in target range for each night separately.
Target range is defined to be between 4.0 and 8.0 mmol/L.
|
8 hours
|
|
Percentage of time in target range for the pooled data
Tidsram: 8 hours
|
Percentage of time for which glucose levels are in target range for the pooled data.
Target range is defined to be between 4.0 to 8.0 mmol/L.
|
8 hours
|
|
Percentage of time spent below 4.0 mmol/L
Tidsram: 8 hours
|
Percentage of time for which glucose levels are below 4.0 mmol/L.
|
8 hours
|
|
Percentage of time spent below 3.3 mmol/L
Tidsram: 8 hours
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Percentage of time for which glucose levels are spent below 3.3 mmol/L.
|
8 hours
|
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Area under the curve for glucose levels below 4.0 mmol/L
Tidsram: 8 hours
|
8 hours
|
|
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Area under the curve for glucose levels below 3.3 mmol/L
Tidsram: 8 hours
|
8 hours
|
|
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Percentage of time spent above 8.0 mmol/L
Tidsram: 8 hours
|
Percentage of time for which glucose levels are above 8.0 mmol/L
|
8 hours
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Percentage of time spent above 10.0 mmol/L
Tidsram: 8 hours
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Percentage of time for which glucose levels are above 10.0 mmol/L.
|
8 hours
|
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Area under the curve for glucose levels spent above 8.0 mmol/L
Tidsram: 8 hours
|
8 hours
|
|
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Area under the curve for glucose levels spent above 10.0 mmol/L
Tidsram: 8 hours
|
8 hours
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|
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Mean glucose levels
Tidsram: 8 hours
|
8 hours
|
|
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Standard deviation of glucose levels
Tidsram: 8 hours
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Standard deviation of glucose levels as a measure of glucose variability.
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8 hours
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Total insulin delivery
Tidsram: 8 hours
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8 hours
|
|
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Number of subjects experiencing at least one hypoglycemic event requiring treatment
Tidsram: 8 hours
|
8 hours
|
|
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Number of hypoglycemic events requiring treatment
Tidsram: 8 hours
|
8 hours
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Samarbetspartners och utredare
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Samarbetspartners
Utredare
- Huvudutredare: Bruce Perkins, Mount Sinai Hospital
Publikationer och användbara länkar
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Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 juli 2013
Primärt slutförande (Faktisk)
1 september 2014
Avslutad studie (Faktisk)
1 september 2014
Studieregistreringsdatum
Först inskickad
12 juli 2013
Först inskickad som uppfyllde QC-kriterierna
17 juli 2013
Första postat (Uppskatta)
22 juli 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
21 oktober 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
18 oktober 2014
Senast verifierad
1 oktober 2014
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- CLASS-04
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