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Closing the Loop in Adults With Type 1 Diabetes - Alcohol Consumption (ANGELA02)

U

University of Cambridge

Status

Completed

Conditions

Type 1 Diabetes

Treatments

Device: Closed loop
Device: Conventional insulin pump delivery

Study type

Interventional

Funder types

Other

Identifiers

NCT00944619
09/H0306/44

Details and patient eligibility

About

The main objective is to assess the efficacy and safety of overnight automated closed loop glucose control using a computer-based algorithm compared with conventional insulin pump therapy in adults with type 1 diabetes following the consumption of a moderate amount of alcohol at dinnertime.

Full description

People with type 1 diabetes need regular insulin injections or continuous delivery of insulin using an insulin pump. Keeping blood sugars in the normal range is known to reduce the risk of long term complications involving the eyes, kidneys and heart. However, achieving treatment goals can be very difficult as the tighter we try to control blood glucose levels, the greater the risk of the person developing episodes of low glucose levels (hypoglycaemia). One solution is using a system where the amount of insulin injected closely matches the blood sugar levels on a continuous basis. This can be achieved by what is known as a "closed loop system" where a small glucose sensor placed under the skin communicates with a computer containing an algorithm that drives a subcutaneous insulin pump. This system is being developed in Cambridge and is undergoing trials in children and adults with type 1 diabetes. Results thus far show that the system is very effective at preventing hypoglycaemia and maintaining blood glucose levels in target range.

We plan to test the closed loop in various challenging conditions faced by patients in daily life. One of these is the consumption of alcohol, which can give rise to delayed hypoglycaemia in patients with diabetes. The studies will be done in a clinical research facility under supervised conditions. Subjects will attend for two study nights where they will receive a specific volume of alcohol with an evening meal. On one night this will be followed by closed loop algorithm control of their insulin overnight. On the other (control) night subjects will remain on their usual pump therapy regime overnight.

Enrollment

12 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Type 1 diabetes, as defined by WHO for at least 6 months or confirmed C-peptide negative
  • On insulin pump therapy for at least 3 months

Exclusion criteria

  • Non-type 1 diabetes mellitus
  • Any physical/psychological disease likely to interfere with the study
  • Taking medication likely to interfere with interpretation of results
  • Known/suspected allergy against insulin
  • Clinically significant nephropathy, neuropathy or retinopathy as judged by the investigator
  • Unstable blood glucose control, including recurrent severe hypoglycaemia as judged by the investigator
  • Current pregnancy/breastfeeding
  • Total daily insulin dose > 1.4 IU/kg
  • HbA1C > 10% within the last 3 months
  • Unable/unwilling to consume the necessary quantity of alcohol stated in the study protocol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

12 participants in 2 patient groups, including a placebo group

Closed loop (algorithm)
Experimental group
Description:
Subcutaneous delivery of Novorapid insulin, dose calculated by computer-driven control algorithm, based on continuous glucose sensor readings
Treatment:
Device: Closed loop
Open loop
Placebo Comparator group
Description:
Subcutaneous delivery of Novorapid insulin according to usual pump regime
Treatment:
Device: Conventional insulin pump delivery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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