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Trial registered on ANZCTR
Registration number
ACTRN12613000070730
Ethics application status
Not yet submitted
Date submitted
17/01/2013
Date registered
18/01/2013
Date last updated
18/01/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Vitamin D in critically ill patients with sepsis in Central Australia
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Scientific title
Measuring Vitamin D levels in patients admitted with sepsis and non sepsis in Central Australia to see if there is any difference in Vitamin D levels in these two groups
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Secondary ID [1]
281789
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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:
Hypovitaminosis D
288112
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Sepsis
288113
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Condition category
Condition code
Metabolic and Endocrine
288487
288487
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0
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Other metabolic disorders
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Infection
288488
288488
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0
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Other infectious diseases
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Intervention/exposure
Study type
Observational
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Patient registry
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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
Measuring Vitamin D level in patients admitted to Intensive care unit and High dependency unit.
Vitamin levels will be measured in blood samples taken on admission. It will be done once during patients admission.
Trial will commence from 1st March 2013 and continue till 31st December 2013
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Intervention code [1]
286331
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Not applicable
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Comparator / control treatment
All patients admitted to ICU/ HDU
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Incidence of hypovitaminosis D in critically ill patients.
Hypovitaminosis D is defined as Vitamin D levels in bloos samples less than 30ng/ml/
To see if there is any difference in vitamin D levels in septic and non-septic patients
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Assessment method [1]
288651
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Timepoint [1]
288651
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baseline on admission to ICU/HDU
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Secondary outcome [1]
300699
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incidence of sepsis in patients admitted to ICU/HDU. This be assessed based on clinical assessment of patient along with blood results obtained from laboratory
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Assessment method [1]
300699
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Timepoint [1]
300699
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with first 24 hrs of admission
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Eligibility
Key inclusion criteria
all patients admitted to ICU/HDU and expected to stay for > 48hrs
> 18 yrs
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Minimum age
18
Years
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Maximum age
No limit
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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
patients expected to stay for < 48 hrs
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/03/2013
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NT
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Recruitment hospital [1]
425
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Alice Springs Hospital - Alice Springs
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Recruitment postcode(s) [1]
6187
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0870 - Alice Springs
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Funding & Sponsors
Funding source category [1]
286576
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Self funded/Unfunded
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Name [1]
286576
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Address [1]
286576
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Country [1]
286576
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Primary sponsor type
Individual
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Name
RAJENDRA GOUD
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Address
PO Box:2234
Alice Springs Hospital
Alice Springs, NT-0870
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Country
Australia
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Secondary sponsor category [1]
285360
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None
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Name [1]
285360
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none
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Address [1]
285360
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Country [1]
285360
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
288645
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Central Australian Human Research Ethics Committee
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Ethics committee address [1]
288645
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PO Box 4066 Alice Springs NT 0871
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Ethics committee country [1]
288645
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Australia
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Date submitted for ethics approval [1]
288645
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28/01/2013
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Approval date [1]
288645
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Ethics approval number [1]
288645
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Summary
Brief summary
Indigenous Australians comprise a major proportion of the Central Australia population and there are a number of issues relating to those requiring critical care for sepsis, including higher rates of bacteraemia and poorer socio-economic status compared with non-indigenous populations in Australia. Despite high sunlight exposure in this region, it is thought that a combination of factors is likely to contribute to lower vitamin D levels among this population. The study will aim to establish baseline vitamin D levels in critically ill patients with sepsis in a Central Australian population. Our hypothesis is that there will be a significant degree of vitamin D deficiency in the critically ill, particularly among the septic cohort, and that it may be so prevalent as to justify routine supplementation in all critically ill patients without prior screening, further down the track
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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
37102
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Dr Rajendra Goud
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Address
37102
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PO Box:2234
Alice Springs Hospital
Alice Springs, NT-0870
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Country
37102
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Australia
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Phone
37102
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+61889517696
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Fax
37102
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Email
37102
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[email protected]
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Contact person for public queries
Name
37103
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Rajendra Goud
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Address
37103
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PO Box:2234
Alice Springs Hospital
Alice Springs, NT-0870
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Country
37103
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Australia
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Phone
37103
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+61889517696
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Fax
37103
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Email
37103
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[email protected]
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Contact person for scientific queries
Name
37104
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Rajendra Goud
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Address
37104
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Po Box: 2234
Alice Springs Hospital
Alice Springs, NT-0870
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Country
37104
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Australia
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Phone
37104
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+61889517696
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Fax
37104
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Email
37104
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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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