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Trial registered on ANZCTR
Registration number
ACTRN12605000040662
Ethics application status
Approved
Date submitted
25/07/2005
Date registered
25/07/2005
Date last updated
19/01/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Management of CBD Stones At Laparoscopic Cholecystectomy
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Scientific title
Management of CBD stones at laparoscopic cholecystectomy: A NSW collaborative prospective randomised trial to assess the value of transcystically inserted CBD stents to facilitate post-operative ERCP.
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Secondary ID [1]
91
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04/001
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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:
Choledocholithiasis
106
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Condition category
Condition code
Oral and Gastrointestinal
125
125
0
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
Facilitated' (placement of a stent at the time of laparoscopic cholecystectomy) endoscopic retrograde cholangiopancreatography (ERCP).
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Intervention code [1]
56
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Treatment: Other
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Comparator / control treatment
Conventional ERCP - for the removal of stones found in the bile duct at the time of laparoscopic cholecystectomy.
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Control group
Active
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Outcomes
Primary outcome [1]
157
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Safety of facilitated ERCP compared to conventional unfacilitated ERCP
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Assessment method [1]
157
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Timepoint [1]
157
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Assessed by the incidence of pancreatitis post ERCP
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Secondary outcome [1]
345
0
The success rate and morbidity of transcystic exploration for common bile duct stone removal across a broad spectrum of surgeons.
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Assessment method [1]
345
0
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Timepoint [1]
345
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Secondary outcome [2]
346
0
The success rate of transcystic stent placement across a broad spectrum of surgeons.
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Assessment method [2]
346
0
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Timepoint [2]
346
0
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Secondary outcome [3]
347
0
The overall morbidity of post-operative ERCP, with further comparisons of the morbidity of facilitated and conventional ERCP, with and without transcystic exploration of the common bile duct to remove stones.
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Assessment method [3]
347
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Timepoint [3]
347
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Secondary outcome [4]
348
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Hospitalisation time according to treatment group.
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Assessment method [4]
348
0
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Timepoint [4]
348
0
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Secondary outcome [5]
349
0
The incidence of hyperamylasemia after transcystic exploration of the common bile duct, transcystic insertion of a stent or transcystic cholangiography alone.
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Assessment method [5]
349
0
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Timepoint [5]
349
0
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Secondary outcome [6]
350
0
The success rate and complications after choledochotomy for common bile duct stones.
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Assessment method [6]
350
0
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Timepoint [6]
350
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Secondary outcome [7]
351
0
The failure rate of selective common bile duct cannulation for facilitated ERCP as compared to conventional ERCP.
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Assessment method [7]
351
0
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Timepoint [7]
351
0
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Secondary outcome [8]
352
0
Incidence of multiple endoscopic procedures when the common bile duct was not explored at the primary operation and whether or not this is affected by facilitation at ERCP.
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Assessment method [8]
352
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Timepoint [8]
352
0
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Secondary outcome [9]
353
0
Long-term efficacy of techniques used to remove common bile duct stones, as measured by the recurrence of stones in the bile duct.
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Assessment method [9]
353
0
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Timepoint [9]
353
0
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Eligibility
Key inclusion criteria
The patient must be able to give informed consent preoperatively (i.e. elective procedures only). Patients at higher than normal risk of having CBD stones identified at OC: a CBD stone identified at ultrasound; a wide CBD (>6mm) at ultrasound; previous, recent, current cholangitis, jaundice, or biliary pancreatitis; abnormal AST and ALT levels (>2 times normal).
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Minimum age
Not stated
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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
Pregnancy at time of surgery. Patients not fit for surgery. For example: those with acute cholecystitis or persistent obstructive jaundice; patients who have had a previous ERCP and sphincterotomy; those in whom intervention was not technically possible (eg. previous Billroth II gastrectomy).
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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)
Central Telephone Number - random allocation once common bile duct stones are identified at operative cholangiogram.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomisation sequence was generated with a computer program, in blocks. Patients are stratified at the time of randomisation according to whether or not the surgeon attempted to explore the common bile duct transcystically but failed to clear it.
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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
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Date of first participant enrolment
Anticipated
19/07/2004
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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
340
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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]
172
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Self funded/Unfunded
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Name [1]
172
0
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Address [1]
172
0
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Country [1]
172
0
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Primary sponsor type
Government body
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Name
Sydney West Area Health Service
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Address
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Country
Australia
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Secondary sponsor category [1]
124
0
Government body
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Name [1]
124
0
Catholic Health Care Service
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Address [1]
124
0
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Country [1]
124
0
Australia
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Secondary sponsor category [2]
125
0
Government body
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Name [2]
125
0
Greater Western Area Health Service
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Address [2]
125
0
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Country [2]
125
0
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Secondary sponsor category [3]
126
0
Government body
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Name [3]
126
0
Hunter New England Area Health Service
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Address [3]
126
0
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Country [3]
126
0
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Secondary sponsor category [4]
127
0
Government body
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Name [4]
127
0
Northern Sydney/Central Coast Area Health Service
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Address [4]
127
0
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Country [4]
127
0
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Secondary sponsor category [5]
128
0
Government body
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Name [5]
128
0
South Eastern Sydney/Illawarra Area Health Service
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Address [5]
128
0
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Country [5]
128
0
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Secondary sponsor category [6]
129
0
Government body
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Name [6]
129
0
Sydney South West Area Health Service
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Address [6]
129
0
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Country [6]
129
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
923
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Catholic Health Care Service- Hawkesbury District Health Service
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Ethics committee address [1]
923
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Ethics committee country [1]
923
0
Australia
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Date submitted for ethics approval [1]
923
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Approval date [1]
923
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Ethics approval number [1]
923
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Ethics committee name [2]
924
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Greater Western Area Health Service - Dubbo Base Hospital
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Ethics committee address [2]
924
0
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Ethics committee country [2]
924
0
Australia
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Date submitted for ethics approval [2]
924
0
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Approval date [2]
924
0
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Ethics approval number [2]
924
0
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Ethics committee name [3]
925
0
Hunter New England Area Health Service
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Ethics committee address [3]
925
0
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Ethics committee country [3]
925
0
Australia
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Date submitted for ethics approval [3]
925
0
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Approval date [3]
925
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Ethics approval number [3]
925
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Ethics committee name [4]
926
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Northern Sydney/Central Coast Area Health Service - Gosford Hospital,
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Ethics committee address [4]
926
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Ethics committee country [4]
926
0
Australia
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Date submitted for ethics approval [4]
926
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Approval date [4]
926
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Ethics approval number [4]
926
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Ethics committee name [5]
927
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Northern Sydney/Central Coast Area Health Service -Royal North Shore Hospital
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Ethics committee address [5]
927
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Ethics committee country [5]
927
0
Australia
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Date submitted for ethics approval [5]
927
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Approval date [5]
927
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Ethics approval number [5]
927
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Ethics committee name [6]
928
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South Eastern Sydney/Illawarra Area Health Service - Prince of Wales Hospital
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Ethics committee address [6]
928
0
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Ethics committee country [6]
928
0
Australia
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Date submitted for ethics approval [6]
928
0
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Approval date [6]
928
0
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Ethics approval number [6]
928
0
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Ethics committee name [7]
929
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South Eastern Sydney/Illawarra Area Health Service - St George Hospital
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Ethics committee address [7]
929
0
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Ethics committee country [7]
929
0
Australia
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Date submitted for ethics approval [7]
929
0
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Approval date [7]
929
0
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Ethics approval number [7]
929
0
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Ethics committee name [8]
930
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Sydney South West Area Health Service - Bankstown-Lidcombe Hospital
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Ethics committee address [8]
930
0
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Ethics committee country [8]
930
0
Australia
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Date submitted for ethics approval [8]
930
0
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Approval date [8]
930
0
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Ethics approval number [8]
930
0
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Ethics committee name [9]
931
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Sydney South West Area Health Service - Liverpool Hospital
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Ethics committee address [9]
931
0
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Ethics committee country [9]
931
0
Australia
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Date submitted for ethics approval [9]
931
0
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Approval date [9]
931
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Ethics approval number [9]
931
0
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Ethics committee name [10]
932
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Sydney South West Area Health Service -Royal Prince Alfred Hospital
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Ethics committee address [10]
932
0
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Ethics committee country [10]
932
0
Australia
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Date submitted for ethics approval [10]
932
0
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Approval date [10]
932
0
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Ethics approval number [10]
932
0
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Ethics committee name [11]
933
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Sydney West Area Health Service - Blue Mountains District ANZAC Memorial Hospital
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Ethics committee address [11]
933
0
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Ethics committee country [11]
933
0
Australia
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Date submitted for ethics approval [11]
933
0
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Approval date [11]
933
0
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Ethics approval number [11]
933
0
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Ethics committee name [12]
934
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Sydney West Area Health Service - Nepean Hospital
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Ethics committee address [12]
934
0
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Ethics committee country [12]
934
0
Australia
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Date submitted for ethics approval [12]
934
0
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Approval date [12]
934
0
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Ethics approval number [12]
934
0
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Ethics committee name [13]
935
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Sydney West Area Health Service - Westmead Hospital
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Ethics committee address [13]
935
0
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Ethics committee country [13]
935
0
Australia
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Date submitted for ethics approval [13]
935
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Approval date [13]
935
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Ethics approval number [13]
935
0
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Summary
Brief summary
This study is designed to assess whether a new technique called facilitated endoscopic retrograde cholangiopancreatography (ERCP) is or is not superior to conventional ERCP to remove stones found in the bile duct at the time of laparoscopic cholecystectomy. ERCP is an endoscopic procedure used to facilitate the radiological examination and subsequent manipulation of the common bile duct (eg. opening it up, which is called sphincterotomy). Both facilitated and conventional ERCP are performed as a separate procedure after the initial gallbladder surgery. This is a comparative study of these two techniques in a randomised clinical trial. The aim of this randomised clinical trial is to enable surgeons to decide whether placement of a plastic stent at the time of laparoscopic cholecystectomy will improve the success rate and safety of subsequent ERCP and sphincterotomy.
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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
35522
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Address
35522
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Country
35522
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Phone
35522
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Fax
35522
0
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Email
35522
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Contact person for public queries
Name
9245
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Professor Christopher J Martin
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Address
9245
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Department of Surgery
Nepean Hospital
Level 5 South Block
PO Box 63
Penrith NSW 2751
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Country
9245
0
Australia
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Phone
9245
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+61 2 47342608
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Fax
9245
0
+61 2 47343432
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Email
9245
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[email protected]
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Contact person for scientific queries
Name
173
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Professor Christopher J Martin
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Address
173
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Department of Surgery
Nepean Hospital
Level 5 South Block
PO Box 63
Penrith NSW 2751
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Country
173
0
Australia
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Phone
173
0
+61 2 47342608
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Fax
173
0
+61 2 47343432
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Email
173
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.
Download to PDF