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Trial registered on ANZCTR
Registration number
ACTRN12605000113651
Ethics application status
Approved
Date submitted
6/08/2005
Date registered
9/08/2005
Date last updated
2/12/2010
Type of registration
Retrospectively registered
Titles & IDs
Public title
The optimal treatment of obesity: a prospective randomized controlled comparison of best practice medical management versus placement of the Lap-Band System to effect weight loss.
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Scientific title
The optimal treatment of obesity: a prospective randomized controlled comparison of best practice medical management versus placement of the Lap-Band System to effect weight loss.
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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
201
0
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Condition category
Condition code
Diet and Nutrition
224
224
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0
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Obesity
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Obese patients will be randomized to either the medical or surgical group. The medical arm will receive treatment with a VLCD plus ongoing individualized care encompassing other obesity drugs as determined and behaviour modification programs. The surgical arm will receive treatment with the Lap-Band System, a laparoscopic adjustable gastric band. Patients will be followed for two years from randomization.
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Intervention code [1]
133
0
Treatment: Surgery
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Comparator / control treatment
best practice medical management
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Control group
Active
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Outcomes
Primary outcome [1]
272
0
Weight loss.
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Assessment method [1]
272
0
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Timepoint [1]
272
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At 2 years.
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Secondary outcome [1]
606
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Body composition changes
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Assessment method [1]
606
0
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Timepoint [1]
606
0
At 12 and 24 months
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Secondary outcome [2]
607
0
Comorbidity changes
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Assessment method [2]
607
0
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Timepoint [2]
607
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At 12 and 24 months
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Secondary outcome [3]
608
0
Functional status changes
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Assessment method [3]
608
0
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Timepoint [3]
608
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At 12 and 24 months measured by SF36, Beck Depression Inventory and Multidimensional Body-Self Relation Questionnaire.
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Secondary outcome [4]
609
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Side effects and economic evaluation.
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Assessment method [4]
609
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Timepoint [4]
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24 months
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Eligibility
Key inclusion criteria
BMI 30-35, have identifiable problems either medical, physical or psychosocial with this level of obesity, be able to understand the options, the potential benefits and risks, and be able to comply with the requirements of each program.
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Minimum age
20
Years
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Maximum age
45
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
Lack of acceptance of the randomization process, history of previous abdominal surgery which would potentially preclude the laparoscopic placement of the band, medical issues which contra-indicated either arm of the study including acute myocardial infarction within the past 6 months, dementia, active psychosis, concurrent experimental drug use, autoimmune disease, pregnancy, lactation, illicit drug use, excessive alcohol intake, use of drugs known to affect body composition, cytotoxic drugs, internal malignancy or major organ failure, inability to understand the risks, unrealistic expectation of benefits or likelihood of failure to comply with the follow up requirements of either program.
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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)
Intervention recorded and stored in numbered, sealed opaque envelopes organized and maintained by staff member not involved in patient care or scheduling and opened in sequence as randomized.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer 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
Parallel
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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
Completed
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Date of first participant enrolment
Anticipated
1/11/2000
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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]
282
0
University
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Name [1]
282
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Monash University Department of Surgery
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Address [1]
282
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Commercial Road
Melbourne Vic 3004
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Country [1]
282
0
Australia
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Funding source category [2]
283
0
Commercial sector/Industry
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Name [2]
283
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Applied Medical
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Address [2]
283
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1/32 Windorah St
P.O Box 1545,
Stafford City 4053. Qld.
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Country [2]
283
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Australia
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Funding source category [3]
284
0
Commercial sector/Industry
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Name [3]
284
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Inamed Health
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Address [3]
284
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5540 Ekwill Street
Santa Barbara, California, USA 93111
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Country [3]
284
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United States of America
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Funding source category [4]
285
0
Commercial sector/Industry
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Name [4]
285
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Novartis
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Address [4]
285
0
327 -333 Police Rd
Mulgrave 3170
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Country [4]
285
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Australia
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Funding source category [5]
286
0
Commercial sector/Industry
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Name [5]
286
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US Surgical
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Address [5]
286
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150 Glover Avenue,
Norwalk, Connecticut 06856,
USA
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Country [5]
286
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United States of America
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Primary sponsor type
University
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Name
Centre for Obesity Research and Education (CORE)
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Address
Commercial Road
Melbourne Vic 3004
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Country
Australia
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Secondary sponsor category [1]
217
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None
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Name [1]
217
0
none
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Address [1]
217
0
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Country [1]
217
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1136
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The Avenue Hospital
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Ethics committee address [1]
1136
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The Avenue Windsor Vic 3181
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Ethics committee country [1]
1136
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Australia
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Date submitted for ethics approval [1]
1136
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Approval date [1]
1136
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Ethics approval number [1]
1136
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Trial 027
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Ethics committee name [2]
1137
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Alfred Hospital
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Ethics committee address [2]
1137
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Commercial Road Melbourne Vic 3004
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Ethics committee country [2]
1137
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Australia
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Date submitted for ethics approval [2]
1137
0
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Approval date [2]
1137
0
06/01/2000
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Ethics approval number [2]
1137
0
166/99
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Ethics committee name [3]
1138
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Monash University SCERH
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Ethics committee address [3]
1138
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Building 3D, Clayton Campus Wellington Road Clayton
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Ethics committee country [3]
1138
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Australia
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Date submitted for ethics approval [3]
1138
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Approval date [3]
1138
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11/11/2003
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Ethics approval number [3]
1138
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2003/458MC
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Summary
Brief summary
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Trial website
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Trial related presentations / publications
Publications Treatment of mild to moderate obesity with laparoscopic adjustable gastric banding or an intensive medical program: a randomized trial. O'Brien PE. Dixon JB. Laurie C. Skinner S. Proietto J. McNeil J. Strauss B. Marks S. Schachter L. Chapman L. Anderson M. Annals of Internal Medicine. 144(9):625-33, 2006 Dixon JB. Strauss BJ. Laurie C. O'Brien PE. Changes in body composition with weight loss: obese subjects randomized to surgical and medical programs. Obesity. 15(5):1187-98, 2007 Presentations “Treatment of mild to moderate obesity with laparoscopic adjustable gastric banding or an intensive medical program” by Emeritus Professor Paul O’Brien at the International Federation for the Surgery of Obesity (IFSO) Europe meeting, Lyon France, April 2006. “Change in body composition with weight loss: Medical and surgical therapies” by Associate Professor John Dixon at the 2006 International Federation for the Surgery of Obesity (IFSO) meeting in Sydney, Australia.
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Public notes
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Contacts
Principal investigator
Name
35217
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Address
35217
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Country
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Phone
35217
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Fax
35217
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Email
35217
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Contact person for public queries
Name
9322
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Ms Cheryl Laurie
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Address
9322
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Centre for Obesity Research and Education (CORE)
Monash University Medical School
Alfred Hospital
Commercial Road
Melbourne VIC 3004
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Country
9322
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Australia
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Phone
9322
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+61 3 99030721
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Fax
9322
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+61 3 95103365
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Email
9322
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[email protected]
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Contact person for scientific queries
Name
250
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Professor Paul O'Brien
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Address
250
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Centre for Obesity Research and Education (CORE)
Monash University Medical School
Alfred Hospital
Commercial Road
Melbourne VIC 3004
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Country
250
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Australia
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Phone
250
0
+61 3 99030721
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Fax
250
0
+61 3 95103365
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Email
250
0
[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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