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Trial registered on ANZCTR
Registration number
ACTRN12606000364572
Ethics application status
Approved
Date submitted
15/09/2005
Date registered
22/08/2006
Date last updated
22/08/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Impact of smoking on the surgical patient.
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Scientific title
A randomised trial of the effectiveness of opportunistic interventions among patients undergoing elective surgery on smoking cessation.
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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:
Tobacco dependence
1333
0
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Condition category
Condition code
Mental Health
1421
1421
0
0
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Addiction
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants in the intervention arms receive either a single phone call informing them that the hospital is a smoke free environment and advising them of the desirability of quitting smoking preoperatively; or a combination of individual counselling and nicotine replacement therapy and are seen weekly for 6 weeks and fortnightly for 4 weeks (ie 8 intervention sessions in total).
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Intervention code [1]
626
0
None
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Comparator / control treatment
Participants in the control arm receive no intervention.
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Control group
Active
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Outcomes
Primary outcome [1]
1942
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Smoking
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Assessment method [1]
1942
0
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Timepoint [1]
1942
0
At Date of Surgery, and 6 weeks, 3 months and 6 months post surgery
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Secondary outcome [1]
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Nil
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Assessment method [1]
3403
0
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Timepoint [1]
3403
0
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Eligibility
Key inclusion criteria
Nicotine dependence and nicotine tolerance of > 5 cigarettes/day (Fagerstrom test); not currently on NRT; not pregnant/breast feeding; ETOH at recommended safe levels; Social Environment suitable for follow up; not active or unstable medical psychiatric condition; able to meet attendance requirements for study; able and willing to give informed consent; first intervention not < 5 days to DOS; English that does not require an interpreter service, will be given a general anaesthetic.
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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 exclusion criteria
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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 randomisation using tamper-proof envelopes.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Identical envelopes containing group allocation randomly selected from a box
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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 3
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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
1/01/2003
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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
150
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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]
1553
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Hospital
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Name [1]
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The Langton Centre
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Address [1]
1553
0
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Country [1]
1553
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Australia
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Primary sponsor type
Hospital
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Name
The Langton Centre
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Address
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Nil
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Address [1]
1366
0
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Country [1]
1366
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Prince of Wales Hospital
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Ethics committee address [1]
2984
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Ethics committee country [1]
2984
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Australia
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Date submitted for ethics approval [1]
2984
0
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Approval date [1]
2984
0
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Ethics approval number [1]
2984
0
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Summary
Brief summary
All hospitals in NSW are working towards becoming “Smoke Free Environments”. Patients are no longer be able to smoke in hospital. The study aims to analyse: - The effectiveness of opportunistic intervention in smokers about to undergo surgery; Perioperative effects (physiological and physical) of short notice cessation of smoking up to six weeks prior to surgery.
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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
36309
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Address
36309
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Country
36309
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Phone
36309
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Fax
36309
0
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Email
36309
0
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Contact person for public queries
Name
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Ms. Mary-Louise White
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Address
9815
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Prince Of Wales Hospital
Randwick NSW 2031
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Country
9815
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Australia
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Phone
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+61 2 93822791
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Fax
9815
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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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Ms. Mary-Louise White
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Address
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Prince Of Wales Hospital
Randwick NSW 2031
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Country
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Australia
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Phone
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+61 2 93822791
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Fax
743
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Email
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[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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