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Trial registered on ANZCTR
Registration number
ACTRN12615001186549
Ethics application status
Approved
Date submitted
30/05/2007
Date registered
3/11/2015
Date last updated
17/02/2021
Date data sharing statement initially provided
24/09/2019
Date results provided
24/09/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Randomised trial of division vs no division of the short gastric blood vessels during laparoscopic Nissen fundoplication for gastro-oesophageal reflux
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Scientific title
Randomised trial of division vs no division of the short gastric blood vessels during laparoscopic Nissen fundoplication for gastro-oesophageal reflux
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Secondary ID [1]
287766
0
none
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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
2161
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Condition category
Condition code
Oral and Gastrointestinal
2256
2256
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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
All patients undergoing a laparoscopic Nissen fundoplication were randomly assigned to undergo division or no division of the short gastric blood vessels. Following surgery they are followed clinically to assess reflux control and side effects
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Intervention code [1]
1791
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Treatment: Surgery
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Comparator / control treatment
Nissen fundoplication with vs. without shorrt gastric blood vessel division
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Control group
Active
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Outcomes
Primary outcome [1]
3118
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Dysphagia and other symptoms will be determined using a clinical questionairre
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Assessment method [1]
3118
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Timepoint [1]
3118
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At 3 months, and then yearly for 20 years
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Secondary outcome [1]
5235
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nil
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Assessment method [1]
5235
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Timepoint [1]
5235
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nil
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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
No limit
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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 laproscopic Nissen fundoplication
severe 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 method
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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?
The people receiving the treatment/s
The people assessing the outcomes
The people analysing the results/data
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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
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Actual
1/07/1994
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Date of last participant enrolment
Anticipated
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Actual
1/01/1996
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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
103
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Recruitment in Australia
Recruitment state(s)
SA
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Funding & Sponsors
Funding source category [1]
2417
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Government body
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Name [1]
2417
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National Health and Medical Research Council
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Address [1]
2417
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Canberra, Australia
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Country [1]
2417
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Australia
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Primary sponsor type
University
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Name
Dept of Surgery, Flinders University
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Address
Flinders University, South Australia
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Country
Australia
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Secondary sponsor category [1]
2190
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University
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Name [1]
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Dept of Surgery, Adelaide University
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Address [1]
2190
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Adelaide, South Australia
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Country [1]
2190
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
4247
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Royal Adelaide Hospital
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Ethics committee address [1]
4247
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Port Road, Adelaide, SA 5000
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Ethics committee country [1]
4247
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Australia
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Date submitted for ethics approval [1]
4247
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Approval date [1]
4247
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07/04/1994
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Ethics approval number [1]
4247
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940402
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Summary
Brief summary
Patients undergoing laparoscopic Nissen fundoplication were randomly assigned to undergo division or no division of the short gastric blood vessels. The study sought to determine whether or not dysphagia was the same in each group
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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
SA 5042
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Country
27894
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Australia
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Phone
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+61882046086
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Fax
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+61882046130
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Email
27894
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[email protected]
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Contact person for public queries
Name
10980
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Professor David Watson
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Address
10980
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Department of Surgery
Flinders Medical Centre
Bedford Park SA 5042
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Country
10980
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Australia
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Phone
10980
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+61 8 82046086
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Fax
10980
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+61 8 82046130
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Email
10980
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[email protected]
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Contact person for scientific queries
Name
1908
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Professor David Watson
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Address
1908
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Department of Surgery
Flinders Medical Centre
Bedford Park SA 5042
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Country
1908
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Australia
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Phone
1908
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+61 8 82046086
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Fax
1908
0
+61 8 82046130
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Email
1908
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
Trial was commenced over 20 yrs ago and follow-up has now closed
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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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