Skip to content

Defining optimal glucose targets in critically ill patients with pre-existing type 2 diabetes and chronic hyperglycaemia.

Evaluation of acute glycaemia on biomarkers and clinical outcomes in critically ill patients with pre-existing type 2 diabetes and chronic hyperglycaemia.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001274864
Enrollment
83
Registered
2012-12-10
Start date
2012-08-19
Completion date
2013-10-05
Last updated
2021-07-05

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

Conditions

None listed

Brief summary

The purpose of this study is to determine the optimum blood glucose target for critically ill patients with high blood glucose levels. This will be done by changing the insulin protocol in ICU for a period of 6 months to compare to the current standard protocol.

Interventions

The intervention is a change in insulin protocol in the Intensive Care Unit (ICU) patients with chronic hyperglycaemia or poorly controlled pre-existing type 2 diabetes. Patients will be identified by a Hba1c test (glycated haemoglobin) on admission to ICU. Patients with a HbA1c >6.9% (or 51 mmol/mol) will be treated with a new Insulin protocol. This study will be performed sequentially; initially (6 months) the study will observe the current Insulin regimen, followed by a 2nd 6 month period in

The intervention is a change in insulin protocol in the Intensive Care Unit (ICU) patients with chronic hyperglycaemia or poorly controlled pre-existing type 2 diabetes. Patients will be identified by a Hba1c test (glycated haemoglobin) on admission to ICU. Patients with a HbA1c >6.9% (or 51 mmol/mol) will be treated with a new Insulin protocol. This study will be performed sequentially; initially (6 months) the study will observe the current Insulin regimen, followed by a 2nd 6 month period in which the intervention (an altered Insulin regimen) will be implemented. The 2 study periods will be separated by 1 month to prevent patients from the control period being included in the intervention period. The new protocol targets blood glucose levels of 10-14 mmol/L in chronic hyperglycaemic patients and poorly controlled type 2 diabetic patients. The current insulin protocol targets blood glucose levels of 6-10 mmol/L. This will involve a change in practice for the bedside nurse who will administer insulin as required to reach the target blood glucose level. The new protocol will result in the administration of less insulin than the current protocol. All patients (including diabetic patients) with a HbA1c of 6.9% or below will continue with the control Insulin regimen if required.

Sponsors

Dr Adam Deane
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

New admission to ICU HbA1c greater than 6.9% or 51 mmol/mol Anticipated to remain in ICU for 48 hours or greater

Exclusion criteria

HbA1c less than 6.9% Type-1 diabetes. Expected to die within 48 hours Not expected to stay for at least 48 hours Readmission to ICU

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026