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CompletedNCT01359241Angie01Updated Nov 12, 2012

Achieving Normal Glucose In Hospital Settings

An interventional study of closed-loop insulin delivery and Usual diabetes treatment regimen in Dysglycaemia, sponsored by University of Cambridge. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-11-12.

Sponsored by University of Cambridge · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Dysglycaemia

Keywords

  • dysglycemia
  • diabetes
  • closed loop insulin delivery
03

In context

Lead sponsor

University of Cambridge is the lead sponsor of 112 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    closed-loop insulin delivery

    Subcutaneous insulin delivery adjusted according to computer-based algorithm advice, based on continuous glucose sensor readings

    Procedure: closed-loop insulin delivery

  • Active comparator
    Usual diabetes treatment regimen

    Usual non-insulin glucose-lowering medications

    Drug: Usual diabetes treatment regimen

Interventions

  • Procedureclosed-loop insulin delivery

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

  • DrugUsual diabetes treatment regimen

    Usual non-insulin glucose lowering medications

06

What researchers measure

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

07

Study locations

1 site
  • Wellcome Trust Clinical Research Facility, Addenbrooke's Hospital
    Cambridge, CB20QQ, United Kingdom
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 12, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01359241
Lead sponsor
University of Cambridge
Collaborators
Cambridge University Hospitals NHS Foundation Trust
Responsible party
Kavita Kumareswaran (Clinical Research Fellow, University of Cambridge) — Principal investigator
First posted
May 24, 2011
Start date
Nov 2011
Primary completion
Jul 2012
Completion
Jul 2012
Last update
Nov 12, 2012

Study contacts

Roman Hovorka, PhD
principal investigator · University of Cambridge

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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