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Trial registered on ANZCTR
Registration number
ACTRN12613000718741
Ethics application status
Approved
Date submitted
27/06/2013
Date registered
1/07/2013
Date last updated
15/12/2015
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effects of fat and protein ‘pre-loads’ on Gastric Emptying, Small Intestine transit, gut hormones, glycaemia, plasma insulin, haemodynamics, absorption, appetite and Gastrointestinal symptoms in response to a mixed meal after Roux-en-Y Gastric Bypass
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Scientific title
Effects of fat and protein ‘pre-loads’ on GE, SI transit, gut hormones, glycaemia, plasma insulin, haemodynamics, absorption, appetite and GI symptoms in response to a mixed meal after RYGB
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Secondary ID [1]
282727
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none
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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:
Obesity and RYGB surgery
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Condition category
Condition code
Diet and Nutrition
289773
289773
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0
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Obesity
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Surgery
289833
289833
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0
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Other surgery
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Twenty morbidly obese subjects will be studied on 3 occasions, which are separated by at least 4 weeks. The subjects will be randomised into 3 “pre-load” groups, in which they will consume either a control of 30ml of water, or one of two preloads, either 30ml olive oil, or 55g Whey protein (in 100ml soup), 30min before a 50g beef patty meal. the preload is administered at t= -30min and the beef patty at t=0
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Intervention code [1]
287390
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Treatment: Other
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Comparator / control treatment
The control will be consuming 30mL of water before the 50g beef patty meal
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Rate of gastric emptying and small intestinal transit as measured by a Gamma camera that will measure the rate at which the stomach empties a 50 or 200ml glucose drink containing 3g of glucose (3-ortho-methyl-D-gluco-pyranose) and a small amount of radiation (which can be detected by the camera)
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Assessment method [1]
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Timepoint [1]
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Gastric emptying curves (expressed as % of the maximum content of the total stomach) will be derived and the content of the total stomach at t = 0, 15, 30, 45, 60, 75, 90, 120, 150, 180, 210 and 240 mins calculated. The 50% emptying time (T50) will also be obtained.
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Primary outcome [2]
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Plasma concentration of gut hormones (CCK, PYY, ghrelin, GLP-1 and insulin)
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Assessment method [2]
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Timepoint [2]
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Blood samples (approximately 15 ml) will be taken prior (t = -2 mins) to the ingestion of the drink and then at t = 15, 30, 45, 60, 75, 90, 120, 150, 180 and 240 mins
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Primary outcome [3]
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Small intestinal glucose and lipid absorption as measured by a 13C triolein breath test
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Assessment method [3]
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Timepoint [3]
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End-expiratory breath samples will be collected at baseline and every 30 minutes postprandially for 6 hrs.
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Secondary outcome [1]
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Blood glucose concentration and the correlation to the rate of gastric emptying, as measured by a portable blood glucose meter.
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Assessment method [1]
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Timepoint [1]
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Measured at (t = -2 mins) to the ingestion of the drink and then at t = 15, 30, 45, 60, 75, 90, 120, 150, 180 and 240 mins
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Secondary outcome [2]
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Blood pressure and heart rate and the correlation to the rate of gastric emptying, measured with an automated oscillometric BP monitor (DINAMAP ProCare 100)
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Assessment method [2]
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Timepoint [2]
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~3min intervals for the first 2 hours and after that every 10mins for the next 2 hours
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Secondary outcome [3]
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Gastrointestinal symptoms before and during procedure, as measured by a validated visual analogue scales (VAS) and also by a validated 19-point GI symptom questionnaire
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Assessment method [3]
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Timepoint [3]
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VAS is completed at Baseline and then at and then at t = 15, 30, 45, 60, 75, 90, 120, 150, 180 and 240 mins
The validated 19-point GI symptom questionnaire is completed by patient before the procedure on each visit.
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Secondary outcome [4]
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Patient body weight using calibrated mecahnical scales
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Assessment method [4]
303467
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Timepoint [4]
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Measured on each visit before the procedure
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Secondary outcome [5]
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The impacts of pre-loads on patients with and without a history of diabetes mellitus
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Assessment method [5]
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Timepoint [5]
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This will be assessed once all data collection is complete.
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Eligibility
Key inclusion criteria
Subjects who have had have had RYGB (Roux-en-Y Gastric Bypass)
RYGB was performed for at least 6 months ago
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Minimum age
18
Years
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Maximum age
65
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 with a history of severe respiratory, cardiovascular, hepatic and/or renal disease, chronic alcohol abuse or epilepsy (excluded by history)
Subjects requiring medication that may influence gastrointestinal function
No previous history of surgery to the gastrointestinal tract apart from the RYGB or LAGB
Subjects who have been exposed to ionising radiation for research purposes in the past 12 months
Female patients not using appropriate contraceptive method (ie oral contraceptive pill, diaphragm, Depo-Provera hormonal contraceptive injection, intrauterine device (IUD), Norplant method)
Pregnancy and/or breastfeeding mothers
Smoking > 10 cigarettes/day
Alcohol consumption > 20 g/day
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
3/12/2010
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Date of last participant enrolment
Anticipated
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Actual
17/12/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
20
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Accrual to date
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Final
20
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
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The Royal Adelaide Hospital - Adelaide
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Recruitment postcode(s) [1]
7020
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5000 - Adelaide
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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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Australian Government 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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Country [1]
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Australia
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Funding source category [2]
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Hospital
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Name [2]
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Department of Gastroenterology and Hepatology, Royal Adelaide Hospital
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Address [2]
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Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, North Wing Motility Laboratory Q7, Level 7, North Terrace, Adelaide, SA, 5000
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Country [2]
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Australia
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Primary sponsor type
Individual
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Name
Nam Nguyen
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Address
Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, North Wing Motility Laboratory Q7, Level 7, North Terrace, Adelaide, SA, 5000
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Country
Australia
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Department of Gastroenterology and Hepatology, Royal Adelaide Hospital
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Address [1]
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Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, North Wing Motility Laboratory Q7, Level 7, North Terrace, Adelaide, SA, 5000
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Royal Adelaide Hospital Reserach Ethics Comittee
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Ethics committee address [1]
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The Royal Adelaide Hospital Research Ethics Committee Level 3, Hanson Institute IMVS Building North Terrace Adelaide SA 5000
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
289496
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Approval date [1]
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25/08/2010
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Ethics approval number [1]
289496
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100808
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Summary
Brief summary
The current study aims to examine the effects of protein and fat ‘preloads’ of RYGB on GE or SI transit, appetite-related and incretin hormones, GI symptoms and haemodynamics. We hypothesized that when given before a mixed meal, (A) a fat ‘preload’ has no effect on GE but slows SI transit, increases the GLP-1 and PYY responses, reduces glycaemic and insulin responses and attenuates the fall in BP and rises in HR/SMA blood flow, as well as symptoms; and (B) a protein ‘preload’ has no effect on GE but slows SI transit, increases GLP-1 and PYY responses, reduces the glycaemic but increases the insulin response and attenuates the fall in BP and rises in HR/SMA flow and symptoms.
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Trial website
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Trial related presentations / publications
Article: Effects of Fat and Protein Preloads on Pouch Emptying, Intestinal Transit, Glycaemia, Gut Hormones, Glucose Absorption, Blood Pressure and Gastrointestinal Symptoms After Roux-en-Y Gastric Bypass Nam Q Nguyen · Tamara L Debreceni · Carly M Burgstad · Melissa Neo · Max Bellon · Judith M Wishart · Scott Standfield · Dylan Bartholomeusz · Chris K Rayner · Gary Wittert · Michael Horowitz. Obesity Surgery 05/2015; DOI:10.1007/s11695-015-1722-7
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Public notes
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Contacts
Principal investigator
Name
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Dr Nam Q Nguyen
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Address
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Department of Gastroenterology & Hepatology, North Wing Level 7 Q7, Royal Adelaide Hospital, North Terrace, Adelaide, SA 5000
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Country
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Australia
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Phone
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+61 8 8222 2412
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Nam Q Nguyen
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Address
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Department of Gastroenterology & Hepatology, North Wing Level 7 Q7, Royal Adelaide Hospital, North Terrace, Adelaide, SA 5000
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Country
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Australia
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Phone
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+61 8 8222 2412
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Nam Q Nguyen
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Address
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Department of Gastroenterology & Hepatology, North Wing Level 7 Q7, Royal Adelaide Hospital, North Terrace, Adelaide SA 5000
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Country
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Australia
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Phone
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+61 8 8222 2412
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Fax
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Email
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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.
Download to PDF