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Trial registered on ANZCTR
Registration number
ACTRN12610000451000
Ethics application status
Approved
Date submitted
27/05/2010
Date registered
2/06/2010
Date last updated
15/12/2015
Type of registration
Prospectively registered
Titles & IDs
Public title
Effects of bariatric surgery on gastrointestinal function.
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Scientific title
Prospective evaluation of healthy volunteers and patients following Roux-en-Y gastric bypass (RYGB) and laparoscopic adjustable gastric banding (LAGB) and the effects on gastric emptying, small intestinal transit, gut hormones, glycaemia, plasma insulin, haemodynamics, absorption, appetite, gastrointestinal symptoms, plasma lipids and body weight
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Secondary ID [1]
251871
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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:
Obesity
257466
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Condition category
Condition code
Oral and Gastrointestinal
257616
257616
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0
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Normal oral and gastrointestinal development and function
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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
Effect of Roux-en-Y gastric bypass (RYGB) and laparoscopic adjustable gastric banding (LAGB) on gastric emptying, small intestinal transit, gut hormones, glycaemia, plasma insulin, haemodynamics, absorption, appetite, gastrointestinal (GI) symptoms, plasma lipids and body weight.
Gastric emptying and small intestinal transit will be measured using scintigraphy
Gut hormones, glycaemia and plasma insulin will be measured by taking blood samples
Plasma lipid and glucose absorption measured using a 13C triolein breath test and 3-O-methyl-glucose (3-OMG) respectively.
Appetite and gastrointestinal symptoms will be measured using questionnaires.
This is a prospective longitudinal study in which all obese subjects will be studied on 4 occasions: 6-8 weeks before surgery (to avoid the pre-operative dietary restriction period), and at 1, 6 and 12 months after surgery; controls will be studied once. Each study will be 6hours in duration.
A group of 20 age- and gender- matched lean volunteers will serve as the “control group”, to provide “normal data” for which the results from the patients’ will be compared. The healthy subjects will only be studied once, with similar concurrent measurements of gastric emptying, gut hormones, blood glucose, blood pressure, heart rate and gastrointestinal symptoms as the surgical subjects.
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Intervention code [1]
256556
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Not applicable
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Comparator / control treatment
Data comparison between bariatric surgery (banding vs. bypass) patient cohorts.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The main aim of the current study is to determine and compare the impact of RYGB and LAGB on gastric emptying (GE) and small intestinal (SI) transit.
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Assessment method [1]
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Timepoint [1]
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Physiological studies will be conducted on 4 occasions: 6-8 weeks before surgery (to avoid the pre-operative dietary restriction period), and at 1, 6 and 12 months after surgery. The rate of GE and SI transit will be measured using scintigraphy for the entire 6 hour duration of the study
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Primary outcome [2]
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Determine and compare the impact of RYGB and LAGB on plasma concentration of gut hormones (Cholecystokinin peptide YY, ghrelin, glucagon-like peptide-1 and insulin)
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Assessment method [2]
258554
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Timepoint [2]
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Measured by taking blood samples every 15mins for the first 2 hours of the study and every 30mins for the following 2 hours of the study
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Primary outcome [3]
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Determine and compare the impact of RYGB and LAGB on small intestinal glucose and lipid absorption
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Assessment method [3]
258555
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Timepoint [3]
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Three grams of 3-O-methyl-glucose (3-OMG) and 200 microlitres of triolein will be added to the test meal to assess small intestinal absorption of glucose and lipid. A 13C triolein breath test will be performed to assess small intestinal lipid absorption. 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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Determine and compare the impact of RYGB and LAGB on blood glucose concentration and the correlation to the rate of gastric emptying
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Assessment method [1]
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Timepoint [1]
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Blood glucose concentrations will be immediately determined using a portable blood glucose meter every 15mins for the first 2 hours of the study and every 30mins of the study there after.
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Secondary outcome [2]
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Determine and compare the impact of RYGB and LAGB on blood pressure (BP) and heart rate (HR) and the correlation to the rate of gastric emptying.
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Assessment method [2]
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Timepoint [2]
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BP (systolic and diastolic) and HR will also be measured with an automated oscillometric BP monitor (DINAMAP ProCare 100) at 3min intervals for the first 2 hours of the study and every 10mins for the following 2 hours
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Secondary outcome [3]
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Gastrointestinal symptoms and quality of life (QOL) will also be recorded in both RYGB and LAGB participants
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Assessment method [3]
264402
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Timepoint [3]
264402
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Gastrointestinal symptoms and QOL will be measured on study days using questionnaires
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Eligibility
Key inclusion criteria
Body Mass Index (BMI) =40kg/m2; or BMI of between 35kg/m2 and 40kg/m2 with other significant disease
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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?
Yes
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Key exclusion criteria
- Medical history: respiratory, cardiovascular, hepatic and/or renal disease
- Chronic alcohol abuse
- epilepsy
- medication known to affect gastrointestinal function
- previous gastrointestinal surgrey (excluding obesity surgery)
- Patients with diabetes mellitus requiring oral hypoglycaemic medication and/or insulin
- exposure to ionising radiation for research purposes in past 12 months
- Females not using appropriate contraceptive method
- Pregnant/breast feeding mothers
- Smoking > 10 cigarettes / day
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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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
27/05/2010
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Actual
10/06/2010
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Date of last participant enrolment
Anticipated
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Actual
10/10/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
110
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Accrual to date
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Final
37
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
2932
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5000
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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 & Medical Research Council
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Address [1]
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GPO Box 1421
Canberra ACT 2601
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
Royal Adelaide Hospital
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Address
North Terrace
Adelaide SA 5000
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Country
Australia
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Secondary sponsor category [1]
256341
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None
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Name [1]
256341
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Address [1]
256341
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Country [1]
256341
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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 Research Ethics Committee
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Ethics committee address [1]
259090
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North Terrace Adelaide SA 5000
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Ethics committee country [1]
259090
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Australia
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Date submitted for ethics approval [1]
259090
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Approval date [1]
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16/04/2010
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Ethics approval number [1]
259090
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091124
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Summary
Brief summary
The main aim of the current study is to determine and compare the impact of laproscopic Roux-en-Y gastric bypass (RYGB) and laproscopic adjustable gastric banding (LAGB) on gastric emptying (GE), small intestinal (SI) transit, gut hormones, glycaemia, plasma insulin, haemodynamics, absorption, appetite, gastrointestinal (GI) symptoms, plasma lipids and body weight.
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Trial website
Nil
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Trial related presentations / publications
Outcomes of Roux-en-Y gastric bypass and laparoscopic adjustable gastric banding Nam Q Nguyen, Tamara L Debreceni, Melissa Neo, Carly M Burgstad, Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, South Australia 5000, Australia. World Journal of Gastroenterology (Impact Factor: 2.37). 09/2013; 19(36):6035-6043. DOI: 10.3748/wjg.v19.i36.6035
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Nam Nguyen
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Address
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Department of Gastroenterology
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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+61422113598
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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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Jenna Burgess
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Address
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Q7 Motility Laboratory
Department Gastroenterology & Hepatology
Level 7, North Wing
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 5214
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Fax
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+61 8 8222 5885
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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 Nguyen
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Address
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Q7 Motility Laboratory
Department Gastroenterology & Hepatology
Level 7, North Wing
North Terrace
Adelaide SA 5000
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Country
5400
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Australia
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Phone
5400
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+61422113598
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Fax
5400
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+61 8 8222 5885
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Email
5400
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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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