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Completed

NCT Number: NCT00944619

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Addenbrooke's Hospital

Cambridge, CB2 0QQ, United Kingdom

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Closed Loop

Device

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

Conventional insulin pump delivery

Device

Subcutaneous delivery of Novorapid insulin according to usual pump regime

Primary outcomes

  1. Percentage of plasma glucose values in target (3.9-8.0 mmol/L)

    Time frame: 2200-1200hr

Secondary outcomes

  1. Percentage of CGM (continuous glucose monitoring) values in target (3.9-8.0 mmol/L)

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  2. Percentage of plasma glucose and CGM values in target (3.9-8.0 mmol/L)

    Time frame: 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  3. Percentage of plasma glucose and CGM values below 3.9 mmol/L

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  4. Percentage of plasma glucose and CGM values above 8.0 mmol/L

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  5. Average plasma and CGM glucose

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  6. Average plasma insulin concentration

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  7. Total dose of insulin administered

    Time frame: 2200-1200hrs

  8. Low blood glucose index (LBGI) score

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  9. High blood glucose index (HBGI) score

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

  10. Percentage of plasma glucose and CGM values below 3.0 mmol/L

    Time frame: 2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

Sponsors and collaborators

Lead sponsor

University of Cambridge

Other

Collaborators

  • Cambridge University Hospitals NHS Foundation Trust

Registry information

Official study title

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

Acronym: ANGELA02

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Jul 23, 2009
Registry last updated
May 12, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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