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Trial registered on ANZCTR
Registration number
ACTRN12607000133437
Ethics application status
Not yet submitted
Date submitted
16/02/2007
Date registered
19/02/2007
Date last updated
19/02/2007
Type of registration
Prospectively registered
Titles & IDs
Public title
Differences in weight loss using a very low energy diet in obese people with and without diabetes.
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Scientific title
In obese subjects with and without diabetes, examining the effect of a very low energy diet (VLED) on weight loss and differences in changes in cardiovascular risk, markers of oxidative stress and advanced glycation, and target organ function.
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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
1625
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Diabetes
1626
0
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Condition category
Condition code
Diet and Nutrition
1733
1733
0
0
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Obesity
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Metabolic and Endocrine
1734
1734
0
0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A very low energy diet (Optifast). This is a meal replacement diet involving three sachets daily plus one serve of vegetables or salad (600-800kcal/day) for 12 weeks (intensive phase). Subsequently patients are weaned over 8 weeks onto a calorie controlled CSIRO-type diet.
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Intervention code [1]
1608
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Lifestyle
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Comparator / control treatment
No comparator.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Change in body composition
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Assessment method [1]
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Timepoint [1]
2408
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At 24 weeks
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Primary outcome [2]
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Change in markers of oxidative stress
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Assessment method [2]
2409
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Timepoint [2]
2409
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At 24 weeks
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Primary outcome [3]
2410
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Change in markers of advanced glycation
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Assessment method [3]
2410
0
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Timepoint [3]
2410
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At 24 weeks
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Primary outcome [4]
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Change in target organ function
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Assessment method [4]
2411
0
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Timepoint [4]
2411
0
At 24 weeks
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Secondary outcome [1]
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Difference in weight loss
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Assessment method [1]
4187
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Timepoint [1]
4187
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At 24 weeks
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Eligibility
Key inclusion criteria
BMI 30 - 50 kg/m2, diabetes and no diabetes.
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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
Thiazolidinedione therapy, significant comorbidity, previously failed VLED or bariatric surgery.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised 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
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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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
1/04/2007
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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
80
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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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Commercial sector/Industry
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Name [1]
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Pfizer CVL grant
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Address [1]
1883
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Country [1]
1883
0
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Funding source category [2]
1884
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Hospital
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Name [2]
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Austin Endocrine Centre research fund
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Address [2]
1884
0
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Country [2]
1884
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Australia
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Primary sponsor type
Individual
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Name
George Jerums
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Address
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Country
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Secondary sponsor category [1]
1698
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Individual
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Name [1]
1698
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Joseph Proietto
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Address [1]
1698
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Country [1]
1698
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
3507
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Austin Health
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Ethics committee address [1]
3507
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Ethics committee country [1]
3507
0
Australia
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Date submitted for ethics approval [1]
3507
0
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Approval date [1]
3507
0
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Ethics approval number [1]
3507
0
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Summary
Brief summary
Obesity and type 2 diabetes increase the risk of heart, kidney and other disease. A process called oxidative stress is thought to be critical in triggering metabolic changes found in both obesity and diabetes, and thus is a major cause of developing complications from these conditions. The role of weight loss in reducing markers of oxidative stress has not been compared in obese people with and without diabetes. We predict that weight loss in obese patients with diabetes will reduce oxidative stress, and improve kidney and heart dysfunction, to a greater extent than in obese patients without diabetes.
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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
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Scott Baker
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Address
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Endocrine Centre
Centaur Wing Repatriation Campus
Austin Health
Waterdale Rd, West Heidelberg 3081
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Country
10797
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Australia
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Phone
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03 9496 5489
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Fax
10797
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03 9496 3365
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Email
10797
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[email protected]
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Contact person for scientific queries
Name
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Professor George Jerums
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Address
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Endocrine Centre
Centaur Wing Repatriation Campus
Austin Health
Waterdale Rd, West Heidelberg VIC 3081
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Country
1725
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Australia
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Phone
1725
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03 9496 5489
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Fax
1725
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03 9496 3365
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Email
1725
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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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