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

Primary Purpose

Type 1 Diabetes

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Closed loop
Conventional insulin pump delivery
Sponsored by
University of Cambridge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept 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

Sites / Locations

  • Addenbrooke's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Closed loop (algorithm)

Open loop

Arm Description

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

Subcutaneous delivery of Novorapid insulin according to usual pump regime

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Percentage of CGM (continuous glucose monitoring) values in target (3.9-8.0 mmol/L)
Percentage of plasma glucose and CGM values in target (3.9-8.0 mmol/L)
Percentage of plasma glucose and CGM values below 3.9 mmol/L
Percentage of plasma glucose and CGM values above 8.0 mmol/L
Average plasma and CGM glucose
Average plasma insulin concentration
Total dose of insulin administered
Low blood glucose index (LBGI) score
High blood glucose index (HBGI) score
Percentage of plasma glucose and CGM values below 3.0 mmol/L

Full Information

First Posted
July 21, 2009
Last Updated
May 10, 2010
Sponsor
University of Cambridge
Collaborators
Cambridge University Hospitals NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00944619
Brief Title
Closing the Loop in Adults With Type 1 Diabetes - Alcohol Consumption
Acronym
ANGELA02
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
January 2010
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Cambridge
Collaborators
Cambridge University Hospitals NHS Foundation Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Closed loop (algorithm)
Arm Type
Experimental
Arm Description
Subcutaneous delivery of Novorapid insulin, dose calculated by computer-driven control algorithm, based on continuous glucose sensor readings
Arm Title
Open loop
Arm Type
Placebo Comparator
Arm Description
Subcutaneous delivery of Novorapid insulin according to usual pump regime
Intervention Type
Device
Intervention Name(s)
Closed loop
Intervention Description
Subcutaneous delivery of Novorapid insulin, dose calculated by control algorithm, based on continuous glucose sensor readings
Intervention Type
Device
Intervention Name(s)
Conventional insulin pump delivery
Intervention Description
Subcutaneous delivery of Novorapid insulin according to usual pump regime
Primary Outcome Measure Information:
Title
Percentage of plasma glucose values in target (3.9-8.0 mmol/L)
Time Frame
2200-1200hr
Secondary Outcome Measure Information:
Title
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
Title
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
Title
Percentage of plasma glucose and CGM values below 3.9 mmol/L
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
Percentage of plasma glucose and CGM values above 8.0 mmol/L
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
Average plasma and CGM glucose
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
Average plasma insulin concentration
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
Total dose of insulin administered
Time Frame
2200-1200hrs
Title
Low blood glucose index (LBGI) score
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
High blood glucose index (HBGI) score
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs
Title
Percentage of plasma glucose and CGM values below 3.0 mmol/L
Time Frame
2200-1200; 0000-0400; 0400-0800; 0800-1200; 0300-1200hrs

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark L Evans, MD FRCP
Organizational Affiliation
University of Cambridge, UK
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Roman Hovorka, PhD
Organizational Affiliation
University of Cambridge, UK
Official's Role
Study Director
Facility Information:
Facility Name
Addenbrooke's Hospital
City
Cambridge
ZIP/Postal Code
CB2 0QQ
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
21493665
Citation
Hovorka R, Kumareswaran K, Harris J, Allen JM, Elleri D, Xing D, Kollman C, Nodale M, Murphy HR, Dunger DB, Amiel SA, Heller SR, Wilinska ME, Evans ML. Overnight closed loop insulin delivery (artificial pancreas) in adults with type 1 diabetes: crossover randomised controlled studies. BMJ. 2011 Apr 13;342:d1855. doi: 10.1136/bmj.d1855.
Results Reference
derived

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

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