Ignite Creation Date:
2024-05-05 @ 12:02 PM
Last Modification Date:
2024-10-26 @ 9:19 AM
Study NCT ID:
NCT00220987
Status:
COMPLETED
Last Update Posted:
2009-01-29
First Post:
2005-09-13
Brief Title:
Normoglycaemia in Intensive Care Evaluation and Survival Using Glucose Algorithm Regulation NICE - SUGAR STUDY
Sponsor:
The George Institute
Organization:
The George Institute
Study Overview
Official Title:
A Multi-Center Open Label Randomized Stratified Controlled Trial of the Effects of Blood Glucose Management on 90-Day All-Cause Mortality in a Heterogenous Population of Intensive Care Unit ICU Patients
Status:
COMPLETED
Status Verified Date:
2009-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The primary aim of the study is to compare the effects of the two blood glucose targets on 90 day all-cause mortality in Intensive Care patients who are predicted on admission to stay in the ICU for at least one full calendar day The hypothesis is that there is little difference in the relative risk of death between patients assigned a glucose range of 45 - 60 mmolL and those assigned a glucose range of less than 100 mmolL with insulin being infused if blood glucose exceeds 100 mmolL and adjusted when needed to maintain blood glucose of 80 - 100 mmolL
Detailed Description:
The NICE-SUGAR study is a multi-centre open label randomised controlled trial of blood glucose management with an intensive insulin regimen to maintain blood glucose between 45 - 60 mmolL versus an insulin regimen maintaining blood glucose less than 100 mmolL with insulin being infused if blood glucose exceeds 100 mmolL and adjusted when needed to maintain blood glucose between 80 - 100 mmolL
To ensure patient safety the target blood glucose concentration must be closely monitored and the results known to the clinical staff treating the patients As patient safety is paramount it is not possible to blind the clinical staff to treatment allocation In this open-label trial bias will be minimised by ensuring concealment of treatment allocation prior to randomisation The unblinded design risks introducing a systematic difference in some other treatment between the two groups this is unlikely in the ICU setting where many other interventions will be administered simultaneously The primary outcome measure is mortality and therefore not subject to ascertainment bias
Patient recruitment
The treatment effect in Van den Berghes study was limited to patients who stayed in Intensive Care for five days or longer but all ventilated patients were admitted to the study at the time of ICU admission Identifying patients who will stay in the ICU for five days or longer is problematic whereas it is relatively easy to identify patients particularly patients admitted for routine post-operative monitoring who will be discharged alive from the ICU after the day following admission For that reason we propose to consider all patients but exclude those expected to be discharged alive or dead before the end of the day following admission
The attending Intensive Care physician will make this assessment In addition it is essential that patients who will stay in the ICU for greater than the eligible criteria time frame but who have a very low risk of death are excluded For this reason we will exclude patients who are able to eat or who are tube fed due to pre-existing bulbar or laryngeal dysfunction and patients who do not merit an arterial line as part of their normal management
Patients who are moribund and at imminent risk of death brain death or cardiac standstill will be excluded This exclusion is on the basis that treatment allocation can not alter the patients outcome
Sample size and power calculations
The ANZICS adult patient database contains information on mortality of patients staying more than 48 hours in ICUs In the financial years 2000 2001 and 2002 of 43760 patients treated in intensive care for greater than 48 hours for whom complete data were available 9476 died prior to hospital discharge The hospital mortality rate was 22 As we will exclude less sick patients who stay greater than 48 hours and 90-day mortality is the primary outcome measure the study has assumed a 90-day mortality rate of 26 in the control group
A total of 6100 patients will be recruited approximately 5100 of these patients will be recruited from the ANZICS CTG centres and approximately 1000 patients will be recruited in Canada
The George Institute for International Health will take responsibility for the web-based randomisation This will be available 24 hours a day A minimisation program will stratify treatment allocation by type of critical illness medical vs surgical and by country Randomisation will be achieved via a password protected fully secure study website
Study treatments
In the lower range group a continuous infusion of insulin administered by syringe pump will be commenced if the blood glucose concentration exceeds 60 mmolL and the infusion rate will be adjusted to maintain the blood glucose concentration between 45 - 60 mmolL
In the higher range group a continuous infusion of insulin administered by syringe pump will be started if the blood glucose concentration exceeds 100 mmolL and the infusion rate adjusted to keep the blood glucose concentration to less than 100 mmolL and titrated when needed to maintain the blood glucose concentration between 8 - 10 mmolL
Adjustments to the insulin dose will be made based initially on the measurement of whole blood glucose in undiluted arterial blood performed initially at hourly intervals Sampling of arterial blood will require the presence of an intra-arterial catheter in situ for routine clinical management at the time of enrolment The frequency of blood glucose measurement may be reduced to two-hourly and then four hourly once the insulin regimen blood glucose concentration and calorie intake are sufficiently stable
Clinical staff both doctors and nurses in the study ICUs will undergo formal training and familiarisation with the insulin regimens by local study coordinators assisted by staff from the appropriate national study coordinating centre Subsequently the administration of insulin will be adjusted by the intensive care doctors and nurses using the study algorithm accessed via the secure password protected encrypted study website The study algorithm recommends insulin infusion rates whilst allowing clinician discretion ultimate responsibility for the safe and effective use of insulin infusions remains with the treating clinicians
Patients being discharged from the ICU will receive conventional blood glucose management subsequent to discharge
Reducing the Incidence of Hypoglycaemia
A major focus of the research coordinators and principal investigators will be to educate staff on the safe use of both insulin regimens in the study All episodes of biochemical hypoglycaemia will be considered serious adverse events and be reported to the coordinating centre within 24 hours These data will also be reported to the independent data and safety monitoring committee If it apparent that there is an unacceptable incidence of hypoglycaemia either in the study overall or in any particular centre or centres then the study committees will take appropriate steps to reduce the incidence Depending on the timing and cause of the episodes this may include any or all of altering the blood glucose control algorithm altering the nutrition guidelines instituting routine IV glucose supplementation increased education at one or more centres or suspending the study at one or more centres
Discontinuation of randomised treatment
Study treatment will continue until the patient is eating and not requiring supplementary enteral or parenteral nutrition or until the earlier of ICU discharge or death or 90 days after randomisation If during the 90-day follow up period the study treatment is ceased and the patient subsequently deteriorates so that they again satisfy the study entry criteria the study treatment will be recommenced
If at any time during the trial the treating ICU physician deems it in the patients best interest for example if the patient suffers significant or repeated episodes of hypoglycaemia then at the discretion of the treating physician the study treatment can be withdrawn Patients withdrawn from the randomised treatment will be followed up according to the study follow up schedule and analysed according to the intention to treat principle unless they or their legal surrogate specifically requests such follow up be ceased
Ancillary Treatments
Other aspects of patient management are unaffected by study procedures and the treating clinicians will be free to provide whatever care is deemed appropriate and necessary
Outcomes
The principal study outcome will be whether the patient is alive or dead at 90 days This will be determined by the research coordinator at each participating centre The study monitor will verify the source documentation at each monitoring visit As death is such a robust outcome unintended bias in outcome assessment is unlikely Intentional bias would require collusion between the study monitor and research nurses and is considered most unlikely Given the robustness of the outcome measure it is unnecessary to establish a blinded outcome committee
Secondary outcomes also determined over the same period include
Death in the ICU by 28 days and by 90 days
Length of ICU stay
Length of hospital stay
The need for organ support inotropes renal replacement therapy and positive pressure ventilation
Incidence of blood stream infections
Incidence and severity of hypoglycaemia
In the subgroup of patients admitted with diagnosis of traumatic brain injury a follow up to determine long term functional status as determined by Extended Glasgow Outcome Scores GOSE will be collected at Day 90 and Six months
Analysis of results
The George Institute will be conducting the statistical analyses All analyses will be performed on an intention-to-treat basis Baseline and outcome variables will be compared using Students t test Chi squared and the Mann-Whitney U test as appropriate Odds ratios will be estimated using multiple logistic regression analysis Survival analysis will be performed using Kaplan Meier and Coxs proportional hazards regression analysis
An independent statistician will conduct two blinded interim analyses when we have primary outcome data for 2000 and 4000 patients and these will be submitted to the DSMC
Safety and Data Monitoring Committee
An independent Safety and Data Monitoring Committee chaired by Professor Sir Richard Peto at Oxford University comprising experts in clinical trials biostatistics and intensive care has been established The committee will review unblinded data on patient characteristics treatment compliance and study outcomes at two interim analyses availability of primary outcome for 1500 and 3500 patients at any other time point the committee may deem necessary to protect study participants and at the final analysis The committee will be charged with informing the study management committee if at any time there emerges
1 Evidence beyond reasonable doubt of a difference between randomised groups in all cause mortality
2 Evidence likely to change the practice of many clinicians already familiar with the available evidence about the comparative effects of the two blood glucose regimens
While the definition of beyond reasonable doubt will be left to the judgement of the Safety and Data Monitoring Committee other committees have considered that a difference in total mortality between randomised groups of three standard deviations would normally constitute such evidence While a major focus of the Committees brief will be to monitor total mortality they would also be provided data on serious adverse events and would not be precluded from making recommendations based on other outcomes such as cause-specific death or serious non-fatal adverse events
This study will provide reliable evidence about the comparative effects of different targets for blood glucose concentration in patients treated in the Australasian and Canadian intensive care setting This evidence will have direct relevance to decisions about the care of critically ill patients admitted to ICUs in Australia and New Zealand Canada and the rest of the world If the study confirms the treatment effect reported in Van den Berghes study maintaining normoglycaemia would likely become a treatment standard worldwide
To ensure patient safety the target blood glucose concentration must be closely monitored and the results known to the clinical staff treating the patients As patient safety is paramount it is not possible to blind the clinical staff to treatment allocation In this open-label trial bias will be minimised by ensuring concealment of treatment allocation prior to randomisation The unblinded design risks introducing a systematic difference in some other treatment between the two groups this is unlikely in the ICU setting where many other interventions will be administered simultaneously The primary outcome measure is mortality and therefore not subject to ascertainment bias
Patient recruitment
The treatment effect in Van den Berghes study was limited to patients who stayed in Intensive Care for five days or longer but all ventilated patients were admitted to the study at the time of ICU admission Identifying patients who will stay in the ICU for five days or longer is problematic whereas it is relatively easy to identify patients particularly patients admitted for routine post-operative monitoring who will be discharged alive from the ICU after the day following admission For that reason we propose to consider all patients but exclude those expected to be discharged alive or dead before the end of the day following admission
The attending Intensive Care physician will make this assessment In addition it is essential that patients who will stay in the ICU for greater than the eligible criteria time frame but who have a very low risk of death are excluded For this reason we will exclude patients who are able to eat or who are tube fed due to pre-existing bulbar or laryngeal dysfunction and patients who do not merit an arterial line as part of their normal management
Patients who are moribund and at imminent risk of death brain death or cardiac standstill will be excluded This exclusion is on the basis that treatment allocation can not alter the patients outcome
Sample size and power calculations
The ANZICS adult patient database contains information on mortality of patients staying more than 48 hours in ICUs In the financial years 2000 2001 and 2002 of 43760 patients treated in intensive care for greater than 48 hours for whom complete data were available 9476 died prior to hospital discharge The hospital mortality rate was 22 As we will exclude less sick patients who stay greater than 48 hours and 90-day mortality is the primary outcome measure the study has assumed a 90-day mortality rate of 26 in the control group
A total of 6100 patients will be recruited approximately 5100 of these patients will be recruited from the ANZICS CTG centres and approximately 1000 patients will be recruited in Canada
The George Institute for International Health will take responsibility for the web-based randomisation This will be available 24 hours a day A minimisation program will stratify treatment allocation by type of critical illness medical vs surgical and by country Randomisation will be achieved via a password protected fully secure study website
Study treatments
In the lower range group a continuous infusion of insulin administered by syringe pump will be commenced if the blood glucose concentration exceeds 60 mmolL and the infusion rate will be adjusted to maintain the blood glucose concentration between 45 - 60 mmolL
In the higher range group a continuous infusion of insulin administered by syringe pump will be started if the blood glucose concentration exceeds 100 mmolL and the infusion rate adjusted to keep the blood glucose concentration to less than 100 mmolL and titrated when needed to maintain the blood glucose concentration between 8 - 10 mmolL
Adjustments to the insulin dose will be made based initially on the measurement of whole blood glucose in undiluted arterial blood performed initially at hourly intervals Sampling of arterial blood will require the presence of an intra-arterial catheter in situ for routine clinical management at the time of enrolment The frequency of blood glucose measurement may be reduced to two-hourly and then four hourly once the insulin regimen blood glucose concentration and calorie intake are sufficiently stable
Clinical staff both doctors and nurses in the study ICUs will undergo formal training and familiarisation with the insulin regimens by local study coordinators assisted by staff from the appropriate national study coordinating centre Subsequently the administration of insulin will be adjusted by the intensive care doctors and nurses using the study algorithm accessed via the secure password protected encrypted study website The study algorithm recommends insulin infusion rates whilst allowing clinician discretion ultimate responsibility for the safe and effective use of insulin infusions remains with the treating clinicians
Patients being discharged from the ICU will receive conventional blood glucose management subsequent to discharge
Reducing the Incidence of Hypoglycaemia
A major focus of the research coordinators and principal investigators will be to educate staff on the safe use of both insulin regimens in the study All episodes of biochemical hypoglycaemia will be considered serious adverse events and be reported to the coordinating centre within 24 hours These data will also be reported to the independent data and safety monitoring committee If it apparent that there is an unacceptable incidence of hypoglycaemia either in the study overall or in any particular centre or centres then the study committees will take appropriate steps to reduce the incidence Depending on the timing and cause of the episodes this may include any or all of altering the blood glucose control algorithm altering the nutrition guidelines instituting routine IV glucose supplementation increased education at one or more centres or suspending the study at one or more centres
Discontinuation of randomised treatment
Study treatment will continue until the patient is eating and not requiring supplementary enteral or parenteral nutrition or until the earlier of ICU discharge or death or 90 days after randomisation If during the 90-day follow up period the study treatment is ceased and the patient subsequently deteriorates so that they again satisfy the study entry criteria the study treatment will be recommenced
If at any time during the trial the treating ICU physician deems it in the patients best interest for example if the patient suffers significant or repeated episodes of hypoglycaemia then at the discretion of the treating physician the study treatment can be withdrawn Patients withdrawn from the randomised treatment will be followed up according to the study follow up schedule and analysed according to the intention to treat principle unless they or their legal surrogate specifically requests such follow up be ceased
Ancillary Treatments
Other aspects of patient management are unaffected by study procedures and the treating clinicians will be free to provide whatever care is deemed appropriate and necessary
Outcomes
The principal study outcome will be whether the patient is alive or dead at 90 days This will be determined by the research coordinator at each participating centre The study monitor will verify the source documentation at each monitoring visit As death is such a robust outcome unintended bias in outcome assessment is unlikely Intentional bias would require collusion between the study monitor and research nurses and is considered most unlikely Given the robustness of the outcome measure it is unnecessary to establish a blinded outcome committee
Secondary outcomes also determined over the same period include
Death in the ICU by 28 days and by 90 days
Length of ICU stay
Length of hospital stay
The need for organ support inotropes renal replacement therapy and positive pressure ventilation
Incidence of blood stream infections
Incidence and severity of hypoglycaemia
In the subgroup of patients admitted with diagnosis of traumatic brain injury a follow up to determine long term functional status as determined by Extended Glasgow Outcome Scores GOSE will be collected at Day 90 and Six months
Analysis of results
The George Institute will be conducting the statistical analyses All analyses will be performed on an intention-to-treat basis Baseline and outcome variables will be compared using Students t test Chi squared and the Mann-Whitney U test as appropriate Odds ratios will be estimated using multiple logistic regression analysis Survival analysis will be performed using Kaplan Meier and Coxs proportional hazards regression analysis
An independent statistician will conduct two blinded interim analyses when we have primary outcome data for 2000 and 4000 patients and these will be submitted to the DSMC
Safety and Data Monitoring Committee
An independent Safety and Data Monitoring Committee chaired by Professor Sir Richard Peto at Oxford University comprising experts in clinical trials biostatistics and intensive care has been established The committee will review unblinded data on patient characteristics treatment compliance and study outcomes at two interim analyses availability of primary outcome for 1500 and 3500 patients at any other time point the committee may deem necessary to protect study participants and at the final analysis The committee will be charged with informing the study management committee if at any time there emerges
1 Evidence beyond reasonable doubt of a difference between randomised groups in all cause mortality
2 Evidence likely to change the practice of many clinicians already familiar with the available evidence about the comparative effects of the two blood glucose regimens
While the definition of beyond reasonable doubt will be left to the judgement of the Safety and Data Monitoring Committee other committees have considered that a difference in total mortality between randomised groups of three standard deviations would normally constitute such evidence While a major focus of the Committees brief will be to monitor total mortality they would also be provided data on serious adverse events and would not be precluded from making recommendations based on other outcomes such as cause-specific death or serious non-fatal adverse events
This study will provide reliable evidence about the comparative effects of different targets for blood glucose concentration in patients treated in the Australasian and Canadian intensive care setting This evidence will have direct relevance to decisions about the care of critically ill patients admitted to ICUs in Australia and New Zealand Canada and the rest of the world If the study confirms the treatment effect reported in Van den Berghes study maintaining normoglycaemia would likely become a treatment standard worldwide
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NHMRC GRANT - 293201 | None | None | None |