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Trial registered on ANZCTR
Registration number
ACTRN12612000488808
Ethics application status
Approved
Date submitted
11/04/2012
Date registered
3/05/2012
Date last updated
3/05/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Does exogenous glucose-dependent insulinotropic polypeptide (GIP) effect gastric emptying and glycaemic response to small intestinal nutrient in critically ill patients?
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Scientific title
The effect of exogenous glucose-dependent insulinotropic polypeptide (GIP) on gastric emptying and glucose metabolism in critically ill patients
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Secondary ID [1]
280297
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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:
Blood Glucose Control
286253
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Critical illness
286404
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Condition category
Condition code
Metabolic and Endocrine
286474
286474
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0
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Other metabolic disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Study Drug: Glucose-dependent insulinotropic polypeptide (GIP) at 4pmol.kg.min
Infused intravenously at rate of 1ml/min from 0-360mins
Patients will be studied on 2 consecutive days (i.e. 24 hour washout period)
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Intervention code [1]
284649
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Treatment: Drugs
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Comparator / control treatment
Control: 0.9% saline
Infused intravenously at rate of 1ml/min from 0-360mins
Patients will be studied on 2 consecutive days (i.e. 24 hour washout period)
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Control group
Placebo
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Outcomes
Primary outcome [1]
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To determine if exogenous glucose-dependent insulinotropic polypeptide (GIP) will lower fasting and nutrient stimulated glycaemia
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Assessment method [1]
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Timepoint [1]
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Blood glucose will be measured at 30min intervals between t=0-360min
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Secondary outcome [1]
297002
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To evaluate in the critically ill patient, the effects of exogenous glucose-dependent insulinotropic polypeptide (GIP) on gastric emptying
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Assessment method [1]
297002
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Timepoint [1]
297002
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1. Scintigraphy - Measurement of gastric emptying following administration of a test meal labelled with 20MBq 99mTC calcium phytate. Test meal will be given 60mins into the study. Stomach content will be measured at 0, 5, 15, 30, 45, 60, 90, 120, 150, 180, 210, 240 and 200 minutes after the meal
2. Octanoate acid breath test - Octanoic acid will be mixed with the test meal and breath samples will be taken initially every 5mins for the first hour, then every 15mins for the remaining 4 hours
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Secondary outcome [2]
297003
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To evaluate in the critically ill patient, the effects of exogenous glucose-dependent insulinotropic polypeptide (GIP) on glucose absorption
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Assessment method [2]
297003
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Timepoint [2]
297003
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3-O-methyl-glucose (3-OMG) measurement - 3grams of 3-O-methyl-glucose will be incorporated into the test meal. Blood samples will be taken at time 0, 15, 30, 45, 60, 90, 120, 150, 180, 210, 240 and 300mins after the meal is administered
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Secondary outcome [3]
297004
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To evaluate in the critically ill patient, the effects of exogenous glucose-dependent insulinotropic polypeptide (GIP) on insulin and glucagon secretion
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Assessment method [3]
297004
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Timepoint [3]
297004
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1. Insulin will be measured via blood samples taken at time 0, 60, 75, 90, 105, 120, 150, 180, 210, 240, 270, 300 and 360min after study commencement
2. Glucagon will be measured via blood samples taken at time 0, 60, 90, 120, 180, 240, 300 and 360min after study commencement
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Secondary outcome [4]
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To evaluate in the critically ill patient, the effects of exogenous glucose-dependent insulinotropic polypeptide (GIP) on endogenous glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) secretion
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Assessment method [4]
297005
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Timepoint [4]
297005
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Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) will be measured via blood samples taken at time 0, 60, 90, 120, 180, 240, 300 and 360min after study commencement
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Eligibility
Key inclusion criteria
Mechanically ventilated critically ill patients.
Suitable for, or receiving post-pyloric nutrition.
Likely to stay ventilated for at least 48 hours.
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Minimum age
18
Years
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Maximum age
80
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
History of diabetes
Pregnancy
Haemoglobin <80g/L
Contraindication to enteral feeding
Previous surgery to small intestine
Any gastrointestinal surgery during admission
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Patients admitted to the Intensive Care Unit (ICU) of the Royal Adelaide Hospital will be screened. Next of kin will be approached for informed consent. Study drug ,synthetic glucose-dependent insulinotropic polypeptide (GIP) and placebo 0.9% saline will be reconstituted by the Royal Adelaide Hospital Department of Pharmacy, as a solution in 4% albumin. Randomisation will be performed by the Department of Pharmacy, so that on each study day the investigators receive the study drug in a glass bottle coved by black plastic, therefore allocation concealment is maintained
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer sequence generation by the department of pharmacy
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
Phase 2
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
18/04/2012
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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
25
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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National Health and Medical Research Council
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Address [1]
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Level 1
16 Marcus Clarke Street
Canberra ACT 2601
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National Health and Medical Research Council
GPO Box 1421
Canberra ACT 2601
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Country [1]
285071
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Australia
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Primary sponsor type
Individual
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Name
Adam Deane
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Address
Intensive Care Unit
Level 4, Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
Australia
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Secondary sponsor category [1]
283934
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None
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Name [1]
283934
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Address [1]
283934
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Country [1]
283934
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
287082
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Royal Adelaide Hospital Research Ethics Committe
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Ethics committee address [1]
287082
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Level 3 Hanson Institute Royal Adelaide Hospital North Terrace Adelaide SA 5000
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Ethics committee country [1]
287082
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Australia
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Date submitted for ethics approval [1]
287082
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Approval date [1]
287082
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21/02/2012
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Ethics approval number [1]
287082
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111131
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Summary
Brief summary
The primary objective of this study is to establish if exogenous glucose-dependent insulinotropic polypeptide (GIP) has a glucose lowering effect in critically ill patients and whether it effects gastric emptying
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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
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Address
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Country
34041
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Phone
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Fax
34041
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Email
34041
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Contact person for public queries
Name
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Palash Kar
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Address
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Intensive Care Unit
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
17288
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Australia
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Phone
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+61 08 82225649
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Fax
17288
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Email
17288
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[email protected]
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Contact person for scientific queries
Name
8216
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Palash Kar
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Address
8216
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Intensive Care Unit
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
8216
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Australia
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Phone
8216
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+61 08 82225649
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Fax
8216
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Email
8216
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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
Source
Title
Year of Publication
DOI
Embase
Effects of glucose-dependent insulinotropic polypeptide on gastric emptying, glycaemia and insulinaemia during critical illness: A prospective, double blind, randomised, crossover study.
2015
https://dx.doi.org/10.1186/s13054-014-0718-3
N.B. These documents automatically identified may not have been verified by the study sponsor.
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