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OpenTrials
Completed

NCT Number: NCT01359241

Achieving Normal Glucose In Hospital Settings

The main objective of this study is to evaluate the efficacy and safety of 24 hours of closed-loop glucose control compared with standard diabetes treatment, in patients with type 2 diabetes treated by non-insulin glucose-lowering medications. This group is being studied as it is representative of patients with glucose dysregulation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Wellcome Trust Clinical Research Facility, Addenbrooke's Hospital

Cambridge, CB20QQ, United Kingdom

About this study

Algorithm driven closed-loop enables automated subcutaneous delivery of insulin in response to real-time continuous glucose sensor readings. Our studies to date have assessed the safety and efficacy of closed-loop insulin delivery in patients with type 1 diabetes in a controlled setting. For patients with type 2 diabetes treated by diet or non-insulin glucose-lowering medications alone, an episode of acute illness may result in elevated glucose levels necessitating initiation of insulin replacement therapy to optimise glycaemic control. Insulin may also be required in patients with no prior history of diabetes, presenting with 'stress hyperglycaemia'. Closed-loop systems may be of benefit in such insulin-naive patients in whom the optimal dosing regimen is difficult to establish, and may provide a safer method of insulin delivery with the added benefit of continuous monitoring of glucose levels on general hospital wards, thus minimising the likelihood of hyper- and hypoglycaemic events and their known associated worse outcomes.

The study has an open-label, randomised, two-period crossover design. Participants will be randomised to undergo two 24-hour studies in a clinical research facility, during which glucose levels will be controlled by either the computer-based closed-loop algorithm (intervention) or by patients' usual non-insulin glucose-lowering diabetes treatment regimen (control). A continuous glucose sensor will be inserted on arrival for each visit. Participants will consume regular meals (matched on both visits) and carry out daily activities mimicking those occurring in an inpatient setting. Stable glucose isotopes will be administered on the two study occasions to collect data for modeling of glucose turnover around meals and during the overnight period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged 18 years or older
  • Type 2 diabetes for at least 1 year as defined by WHO
  • Treatment with glucose-lowering medication(s) (including Exenatide) for at least 6 mths
  • HbA1c between 7.0% and 10.0% inclusive (measured within past 3 mths)

Exclusion criteria

  • Autoimmune type 1 diabetes
  • Type 2 diabetes treated with insulin
  • Type 2 diabetes treated with diet control alone
  • Known or suspected allergy against insulin
  • Proliferative retinopathy
  • Current or planned pregnancy or breast feeding
  • Any physical or psychological disease or medication(s) likely to interfere with the conduct of the study and interpretation of the study results, as judged by the study clinician

Treatment and study plan

closed-loop insulin delivery

Procedure

Insulin delivery via subcutaneous pump, adjusted according to computer-based algorithm advice, based on continuous glucose sensor readings

Usual diabetes treatment regimen

Drug

Usual non-insulin glucose lowering medications

Primary outcomes

  1. Percent of plasma glucose values within target range 3.9-8.0 mmol/l

    Time frame: 24 hrs

Secondary outcomes

  1. Percent of sensor glucose values within target range 3.9-8.0 mmol/l

    Time frame: 24 hrs

  2. Percent of plasma and sensor glucose values below 3.9 mmol/l

    Time frame: 24 hrs

  3. Percent of plasma and sensor glucose values above 8.0 mmol/l

    Time frame: 24 hrs

  4. Mean plasma and sensor glucose

    Time frame: 24 hrs

  5. Mean plasma insulin concentration

    Time frame: 24 hrs

  6. Total basal insulin insulin delivery

    Time frame: 24 hrs

  7. Low blood glucose index (LBGI) score

    Time frame: 24 hrs

  8. High blood glucose index (HBGI) score

    Time frame: 24 hrs

  9. Hyperglycaemic index score

    Time frame: 24 hrs

  10. Percent of plasma and sensor glucose values below 3.0 mmol/l

    Time frame: 24 hrs

  11. Standard deviation of plasma glucose

    Time frame: 24 hrs

  12. Frequency of hypoglycaemia

    Time frame: 24 hrs

  13. Frequency of hyperglycaemia

    Time frame: 24 hrs

Sponsors and collaborators

Lead sponsor

University of Cambridge

Other

Collaborators

  • Cambridge University Hospitals NHS Foundation Trust

Registry information

Official study title

An Open-label, Single-centre, Randomised, Two-period Crossover Study to Assess the Efficacy and Safety of 24-hour Closed-loop Glucose Control in Comparison With Conventional Treatment in Adults With Type 2 Diabetes on Non-insulin Glucose-lowering Agents

Acronym: Angie01

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
May 24, 2011
Registry last updated
Nov 12, 2012

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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