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Trial registered on ANZCTR
Registration number
ACTRN12605000114640
Ethics application status
Approved
Date submitted
5/08/2005
Date registered
9/08/2005
Date last updated
25/10/2007
Type of registration
Retrospectively registered
Titles & IDs
Public title
Hypofractionated radiotherapy for the palliation of patients with advanced head and neck cancer who are unsuitable for an attempt at curative treatment
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Scientific title
Assessment of quality of life of patients undergoing hypofractionated radiotherapy for the palliation of patients with advanced head and neck cancer who are unsuitable for an attempt at curative treatment
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Secondary ID [1]
107
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Hypofractionated head and neck study
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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:
Advanced head and neck cancer
202
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Condition category
Condition code
Cancer
225
225
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0
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Head and neck
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Hypofractionated radiotherapy, 30 Gray in 5 fractions, optional 6th 5 Gray fraction.
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Intervention code [1]
123
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Treatment: Other
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Comparator / control treatment
None - single arm study
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
273
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Quality of life
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Assessment method [1]
273
0
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Timepoint [1]
273
0
Assessed at baseline, 1, 2, 3, 6, 9 and 12 months post treatment.
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Secondary outcome [1]
610
0
Analgesic requirements and radiation toxicity
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Assessment method [1]
610
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Timepoint [1]
610
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Assessed at baseline, weekly during treatment and at 1, 2, 3, 6, 9 and 12 months post treatment.
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Secondary outcome [2]
611
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Local control
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Assessment method [2]
611
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Timepoint [2]
611
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Assessed at 1, 2, 3, 6, 9 & 12 months post treatment.
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Secondary outcome [3]
612
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Survival
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Assessment method [3]
612
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Timepoint [3]
612
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Assessed up to 12 months post treatment.
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Eligibility
Key inclusion criteria
Biopsy proven squamus cell carcinoma (primary or regional nodal disease) of the head and neck, ineligible for curative treatment, performance status 0-2, life expectanccy of at least 4 months, written informed consent.
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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
No exclusion criteria
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
Single group
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Other design features
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Phase
Phase 2
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Type of endpoint/s
Safety/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
17/08/2004
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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
40
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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]
287
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Self funded/Unfunded
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Name [1]
287
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Address [1]
287
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Country [1]
287
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Primary sponsor type
Individual
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Name
Dr Sandro Porceddu
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Address
Princess Alexandra Hospital
Ipswich Rd
Woolloongabba QLD 4102
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Country
Australia
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Secondary sponsor category [1]
218
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None
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Name [1]
218
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none
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Address [1]
218
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Country [1]
218
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1139
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Southern Zone Radiation Oncology Service-Pricness Alexandra Hospital
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Ethics committee address [1]
1139
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Ethics committee country [1]
1139
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Australia
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Date submitted for ethics approval [1]
1139
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Approval date [1]
1139
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Ethics approval number [1]
1139
0
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Ethics committee name [2]
1140
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Southern Zone Radiation Oncology Service-Mater Hospital,South Brisbane
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Ethics committee address [2]
1140
0
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Ethics committee country [2]
1140
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Australia
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Date submitted for ethics approval [2]
1140
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Approval date [2]
1140
0
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Ethics approval number [2]
1140
0
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Ethics committee name [3]
1141
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The Townsville Hospital
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Ethics committee address [3]
1141
0
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Ethics committee country [3]
1141
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Australia
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Date submitted for ethics approval [3]
1141
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Approval date [3]
1141
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Ethics approval number [3]
1141
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Summary
Brief summary
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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
35798
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Address
35798
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Country
35798
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Phone
35798
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Fax
35798
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Email
35798
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Contact person for public queries
Name
9312
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Dr Sandro Porceddu
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Address
9312
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Radiation Oncology
Princess Alexandra Hospital
Ipswich Rd
Woolloongabba QLD 4102
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Country
9312
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Australia
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Phone
9312
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+61 7 32405279
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Fax
9312
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+61 7 32402252
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Email
9312
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[email protected]
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Contact person for scientific queries
Name
240
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Brenda Rosser
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Address
240
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Oncology Research Unit
Delivery Point 35
Princess Alexandra Hospital
Ipswich Rd
Woolloongabba Brisbane QLD 4102
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Country
240
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Australia
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Phone
240
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+61 7 32402130
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Fax
240
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+61 7 32402252
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Email
240
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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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