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Trial registered on ANZCTR
Registration number
ACTRN12607000303448
Ethics application status
Approved
Date submitted
30/05/2007
Date registered
6/06/2007
Date last updated
2/03/2021
Date data sharing statement initially provided
24/09/2019
Date results provided
24/09/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
A randomised trial of Anterior 180 degree vs Nissen fundoplication to control and assess the contol of reflux and side effects in patients undergonig surgery for gastro-oesophageal reflux
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Scientific title
A randomised trial of Anterior 180 degree vs Nissen fundoplication to control and assess the contol of reflux and side effects in patients undergonig surgery for gastro-oesophageal reflux
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Secondary ID [1]
287804
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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
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Condition category
Condition code
Oral and Gastrointestinal
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1940
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0
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Normal oral and gastrointestinal development and function
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
2 types of fundoplication for gastro-oesophageal reflux compared. 1) Nissen (total) fundoplication 2) Anterior 180 degree partial (stomach sutured across front of oesophagus) fundoplication.
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Intervention code [1]
1792
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Treatment: Surgery
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Comparator / control treatment
Comparison of 2 equally valid procedures in RCT
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Control group
Active
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Outcomes
Primary outcome [1]
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Dysphagia and reflux symptoms will be determined using a clinical questionnaire
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Assessment method [1]
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Timepoint [1]
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At 3 months, and then yearly for 20 years
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Secondary outcome [1]
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Dysphagia and other symptoms will be determined using a clinical questionnaire
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Assessment method [1]
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Timepoint [1]
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At 3 months, and then yearly for 20 years.
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Eligibility
Key inclusion criteria
Suitable for a laparoscopic Nissen fundoplication
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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
Not suitable for laparoscopic Nissen fundoplicationsevere oesophageal motility disorder
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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 opaque envelope technique
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
120 Envelopes prepared by independent nurse (60 = treatment, 60=control), and shuffled extensively.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
patients and nurse undertaking follow-up blinded as to which operation was performed
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Phase
Not Applicable
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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
1/01/1996
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Actual
1/01/1996
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Date of last participant enrolment
Anticipated
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Actual
31/12/1997
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Date of last data collection
Anticipated
1/01/2020
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Actual
1/01/2020
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Sample size
Target
100
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Accrual to date
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Final
107
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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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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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National Health and Medical Research Council
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Address [1]
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Canberra
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Department of Surgery, Flinders University
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Address
Bedford Park, SA
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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Department of Surgery, Adelaide University
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Address [1]
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Adelaide
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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
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Ethics committee address [1]
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Port Road, 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]
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Approval date [1]
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20/04/1995
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Ethics approval number [1]
3873
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950413
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Summary
Brief summary
Random assignment to either Nissen or anterior partial fundoplication. Outcome is relfux control and side effects (especially dysphagia)
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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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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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Professor David Watson
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Address
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Dept of Surgery, Flinders Medical Centre
Bedford Park
SA 5042
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Country
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Australia
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Phone
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08 82046086
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Fax
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08 82046130
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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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Professor David Watson
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Address
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Dept of Surgery
Flinders Medical Centre
Bedford Park
South Australia 5042
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Country
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Australia
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Phone
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08 82046086
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Fax
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08 82046130
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Email
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[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
No additional documents have been identified.
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