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

Randomised, Two-Period Crossover Study to Assess the Efficacy of Overnight Computer-based Glucose Control Compared With Conventional Pump Therapy Following the Consumption of Alcohol in Adults With Type 1 Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00944619
Acronym
ANGELA02
Enrollment
12
Registered
2009-07-23
Start date
2009-09-30
Completion date
2009-12-31
Last updated
2010-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Brief summary

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.

Detailed 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.

Interventions

Subcutaneous delivery of Novorapid insulin, dose calculated by control algorithm, based on continuous glucose sensor readings

Subcutaneous delivery of Novorapid insulin according to usual pump regime

Sponsors

Cambridge University Hospitals NHS Foundation Trust
CollaboratorOTHER
University of Cambridge
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Percentage of plasma glucose values in target (3.9-8.0 mmol/L)2200-1200hr

Secondary

MeasureTime frame
Percentage of plasma glucose and CGM values in target (3.9-8.0 mmol/L)0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Percentage of plasma glucose and CGM values below 3.9 mmol/L2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Percentage of plasma glucose and CGM values above 8.0 mmol/L2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Average plasma and CGM glucose2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Percentage of CGM (continuous glucose monitoring) values in target (3.9-8.0 mmol/L)2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Total dose of insulin administered2200-1200hrs
Low blood glucose index (LBGI) score2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
High blood glucose index (HBGI) score2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Percentage of plasma glucose and CGM values below 3.0 mmol/L2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Average plasma insulin concentration2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026