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Trial registered on ANZCTR
Registration number
ACTRN12616001692426
Ethics application status
Approved
Date submitted
15/11/2016
Date registered
8/12/2016
Date last updated
8/12/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Studies of Glucocorticoid Induced Hyperglycaemia - Part 1: effects of commonly prescribed Glucocorticoid (GC) regimens on blood sugar levels
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Scientific title
Continuous glucose monitoring to profile the effects of Glucocorticoid regimens on glycaemia.
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Secondary ID [1]
290336
0
Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Diabetes
300606
0
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Hyperglycaemia
300607
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Condition category
Condition code
Metabolic and Endocrine
300456
300456
0
0
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Diabetes
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Reproductive Health and Childbirth
300996
300996
0
0
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Antenatal care
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Renal and Urogenital
300997
300997
0
0
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Kidney disease
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
To use continuous glucose monitoring (CGM) to profile the glycemic impact of commonly prescribed Glucocorticoid (GC) regimens. CGM will be applied for 3 days prior to the first dose of GC and continued for 3 days following GC administration at per the prescribed dose frequency (total duration 6 days)
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Intervention code [1]
296148
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Not applicable
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Comparator / control treatment
Internal control; continuous glucose monitoring before and after administration of glucocorticoid
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Control group
Active
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Outcomes
Primary outcome [1]
299893
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Peak interstitial fluid glucose induced by glucocorticoid administration, detected by CGM
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Assessment method [1]
299893
0
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Timepoint [1]
299893
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Within 24 hours of each dose of glucocorticoid administered.
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Secondary outcome [1]
328404
0
Nadir glucose detected by CGM
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Assessment method [1]
328404
0
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Timepoint [1]
328404
0
Within 24 hours of each dose of glucocorticoid administered, detected by CGM
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Secondary outcome [2]
328405
0
glycemic variability as assessed by the J-index calculated from CGM traces
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Assessment method [2]
328405
0
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Timepoint [2]
328405
0
24 hours post each dose of glucocorticoid administered
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Secondary outcome [3]
328406
0
Incidence of hyperglycaemia defined by the time spent with glucose greater than 7.8mmol/L during each 24 hour period post glucocorticoid administration
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Assessment method [3]
328406
0
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Timepoint [3]
328406
0
Within 24 hours of glucocorticoid administration
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Secondary outcome [4]
328407
0
Use of diabetes therapy as documented in the medical record
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Assessment method [4]
328407
0
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Timepoint [4]
328407
0
24 hours post glucocorticoid administration
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Secondary outcome [5]
328408
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Incidence of hypoglycaemia defined by time spent with glucose <4mmol/L during each 24 hour period post glucocorticoid administration
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Assessment method [5]
328408
0
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Timepoint [5]
328408
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24 hours post glucocorticoid administration
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Eligibility
Key inclusion criteria
Patients with and without diabetes who are planned to have glucocorticoids for a medical indication.
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Minimum age
18
Years
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Maximum age
90
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Subjects under the age of 18, subjects whose primary language is other than English, subjects with a cognitive impairment, an intellectual disability or a mental illness
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Descriptive statistics will be percentages for categorical data, mean +/- SD for normally distributed continuous data and median (interquartile range (IQR)) for non-normally distributed continuous or ordinal data. Paired and unpaired t-tests will be used to detect the differences in glycaemia and glycaemic variability between GC therapy and no GC therapy. The Wilcoxon rank test will be used to detect differences in ordinal data. Area under the glucose concentration-time curve will be measured using the trapezoidal rule. Results will be calculated using GraphPad Prism version 6.0a for Mac OS X, GraphPad Software (La Jolla California, USA). P values <0.05 will be considered statistically significant.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
12/12/2016
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Actual
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Date of last participant enrolment
Anticipated
31/12/2018
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Actual
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Date of last data collection
Anticipated
31/12/2018
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Actual
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Sample size
Target
80
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
6937
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Royal Melbourne Hospital - City campus - Parkville
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Recruitment hospital [2]
6938
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Sunshine Hospital - St Albans
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Recruitment hospital [3]
6939
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Footscray Hospital - Footscray
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Recruitment postcode(s) [1]
14619
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3050 - Parkville
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Recruitment postcode(s) [2]
14620
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3021 - St Albans
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Recruitment postcode(s) [3]
14621
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3011 - Footscray
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Funding & Sponsors
Funding source category [1]
294979
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Hospital
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Name [1]
294979
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Western Health Dept Diabetes and Endocrinology
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Address [1]
294979
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Sunshine Hospital
Furlong Rd
St Albans
VIC 3021
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Country [1]
294979
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Australia
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Funding source category [2]
294980
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Hospital
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Name [2]
294980
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Royal Melbourne Hospital
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Address [2]
294980
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Dept Diabetes and Endocrinology
Grattan St
Parkville
VIC 3050
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Country [2]
294980
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Australia
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Primary sponsor type
Hospital
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Name
Western Health Dept Diabetes and Endocrinology
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Address
Dept Diabetes and Endocrinology
Furlong Rd
St Albans
VIC 3021
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Country
Australia
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Secondary sponsor category [1]
293801
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Hospital
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Name [1]
293801
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Melbourne Health
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Address [1]
293801
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Dept Diabetes and Endocrinology
Grattan St
Parkville
VIC 3050
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Country [1]
293801
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
296336
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MHHREC
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Ethics committee address [1]
296336
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Grattan St Parkville VIC 3050
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Ethics committee country [1]
296336
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Australia
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Date submitted for ethics approval [1]
296336
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27/04/2016
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Approval date [1]
296336
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05/09/2016
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Ethics approval number [1]
296336
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HREC/16/MH/128 - 2016.117
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Summary
Brief summary
To use continuous glucose monitoring (CGM) to profile the glycemic impact of commonly prescribed GC regimens.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
69698
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Dr Christopher Yates
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Address
69698
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Dept Diabetes and Endocrinology
Royal Melbourne Hospital
Grattan St
Parkville
VIC 3050
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Country
69698
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Australia
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Phone
69698
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+61 3 93427000
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Fax
69698
0
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Email
69698
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[email protected]
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Contact person for public queries
Name
69699
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Christopher Yates
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Address
69699
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Dept Diabetes and Endocrinology
Royal Melbourne Hospital
Grattan St
Parkville
VIC 3050
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Country
69699
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Australia
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Phone
69699
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+61 3 93427000
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Fax
69699
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Email
69699
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[email protected]
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Contact person for scientific queries
Name
69700
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Christopher Yates
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Address
69700
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Dept Diabetes and Endocrinology
Royal Melbourne Hospital
Grattan St
Parkville
VIC 3050
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Country
69700
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Australia
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Phone
69700
0
+61 3 93427000
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Fax
69700
0
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Email
69700
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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