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Trial registered on ANZCTR
Registration number
ACTRN12605000035628
Ethics application status
Approved
Date submitted
20/07/2005
Date registered
22/07/2005
Date last updated
1/06/2024
Date data sharing statement initially provided
24/09/2019
Date results provided
24/09/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Multicentre Randomised Controlled Trial of Anterior vs Posterior vs Nissen Fundoplication
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Scientific title
Anterior versus Posterior versus Nissen Fundoplication for the control of gastro-oesophageal reflux
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Secondary ID [1]
287837
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Nil Known
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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:
Gastro-oesophageal reflux
98
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Condition category
Condition code
Oral and Gastrointestinal
119
119
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Laparoscopic fundoplication - Anterior vs Posterior vs Nissen Fundoplication
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Intervention code [1]
43
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Treatment: Surgery
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Comparator / control treatment
3 surgical variants compared in RCT
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Control group
Active
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Outcomes
Primary outcome [1]
150
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Control of Reflux
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Assessment method [1]
150
0
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Timepoint [1]
150
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n/a
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Secondary outcome [1]
331
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Side effects
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Assessment method [1]
331
0
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Timepoint [1]
331
0
n/a
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Eligibility
Key inclusion criteria
Proven gastro-oesophageal reflux disease by either endoscopic or 24 hour pH monitoring. Antireflux surgery clinically indicated. Fit for surgery. Reflux inadequately controlled by standard medications or unwilling to take lifelong medication for reflux.
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Minimum age
18
Years
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Maximum age
Not stated
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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
No informed consent. Previous surgery for gastro-oesophageal reflux. Very large hiatus hernia (more than 50% of stomach in the chest). PregnantOesophageal motility disorder which precludes Nissen fundoplication.
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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)
sealed envelope
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
shuffled envelopes
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Masking / blinding
Blinded (masking 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
Active, not recruiting
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Date of first participant enrolment
Anticipated
8/01/2005
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Actual
31/12/2012
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Date of last participant enrolment
Anticipated
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Actual
31/12/2012
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Date of last data collection
Anticipated
31/12/2032
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Actual
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Sample size
Target
100
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Accrual to date
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Final
100
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Recruitment in Australia
Recruitment state(s)
SA
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Funding & Sponsors
Funding source category [1]
164
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Self funded/Unfunded
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Name [1]
164
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Address [1]
164
0
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Country [1]
164
0
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Primary sponsor type
Charities/Societies/Foundations
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Name
ISDE - Australasian section
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Address
No address
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Country
Australia
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Secondary sponsor category [1]
119
0
None
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Name [1]
119
0
nil
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Address [1]
119
0
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Country [1]
119
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
909
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Flinders Medical Centre
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Ethics committee address [1]
909
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Bedford Park, SA, 5042
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Ethics committee country [1]
909
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Australia
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Date submitted for ethics approval [1]
909
0
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Approval date [1]
909
0
01/07/2005
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Ethics approval number [1]
909
0
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Ethics committee name [2]
910
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Royal Adelaide Hopsital
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Ethics committee address [2]
910
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Port Road, Adelaide, SA, 5000
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Ethics committee country [2]
910
0
Australia
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Date submitted for ethics approval [2]
910
0
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Approval date [2]
910
0
01/07/2005
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Ethics approval number [2]
910
0
n/a
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Summary
Brief summary
Multicentre prospective double blind randomized controlled trial comparing 3 surgical procedures for gastro-oesophageal reflux. All groups will undergo a clinically acceptable operation, according to standard clinical indications. The study will be performed in multiple centres throughout Australia and New Zealand. The study will be coordinated from FMC and RAH in SA. Patients will be recruited over a 2 year period. Follow-up will continue for up to 20 years.
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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
35981
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Prof David Watson
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Address
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Dept Surgery
Flinders University
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Country
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Australia
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Phone
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+61882046086
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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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David Watson
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Address
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Department of Surgery
Flinders Medical Centre
Bedford Park SA 5042
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Country
9232
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Australia
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Phone
9232
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+61 8 82046086
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Fax
9232
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+61 8 82046130
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Email
9232
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[email protected]
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Contact person for scientific queries
Name
160
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David Watson
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Address
160
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Department of Surgery
Flinders Medical Centre
Bedford Park SA 5042
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Country
160
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Australia
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Phone
160
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+61 8 82046086
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Fax
160
0
+61 8 82046130
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Email
160
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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
Randomized controlled trial of laparoscopic anterior 180degree partial versus posterior 270degree partial fundoplication.
2015
https://dx.doi.org/10.1111/ans.12476
N.B. These documents automatically identified may not have been verified by the study sponsor.
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