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Trial registered on ANZCTR
Registration number
ACTRN12609000304235
Ethics application status
Not yet submitted
Date submitted
14/04/2009
Date registered
19/05/2009
Date last updated
19/05/2009
Type of registration
Prospectively registered
Titles & IDs
Public title
Bronchoscopic detection of sentinel lymph node in non-small cell lung cancer: a feasibility study
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Scientific title
A feasibility study in developing a novel technique for bronchoscopic detection of sentinel lymph node in non-small cell lung cancer patients
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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:
Non-small cell lung cancer
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Condition category
Condition code
Cancer
4884
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0
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Lung - Non small cell
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Bronchoscopic injection, via transbronchial needle introduced into submucosal layer of bronchial wall, of technetium-99 (antimony colloid) into region of lung in which lung cancer resides.
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Intervention code [1]
4354
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Diagnosis / Prognosis
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Comparator / control treatment
None - feasibility study
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Identification of sentinel lymph node by non-invasive means using Nuclear Medicine imaging
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Assessment method [1]
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Timepoint [1]
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24 hours after bronchoscopy
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Secondary outcome [1]
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Safety: risk of pneumothorax
Mode of assessment of outcome: Routine chest x-ray will be performed after each procedure. clinical observatino for a minimum 4 hours post-procedure will also be routine
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Assessment method [1]
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Timepoint [1]
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4 hours after bronchoscopy
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Eligibility
Key inclusion criteria
patients undergoing flexible bronchoscopy for the diagnosis of suspected peripheral lung cancer
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Minimum age
40
Years
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Maximum age
85
Years
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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
Patient declines
Mediastinal lymphadenopathy on computerized tomography (CT) chest
medically unsuitable for bronchoscopy
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Study design
Purpose of the study
Diagnosis
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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
Bronchoscopic injection of Technetium-99 into carina of lung lobe in which lung mass is stiuated will be performed following diagnostic sampling.
Single Photon Emission computerized tomography combined with conventional computerized tomography (SPECT/CT) chest will be performed in order to visualize drainage of radio-isotope to regional lymph nodes in order to identify sentinel node.
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/07/2009
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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
10
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Daniel Steinfort
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Address
c/- Dept Respiratory Medicine
Royal Melbourne Hospital
Grattan St
Parkville
Victoria 3050
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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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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
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Ethics committee address [1]
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Ethics committee country [1]
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Date submitted for ethics approval [1]
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24/04/2009
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Approval date [1]
6822
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Ethics approval number [1]
6822
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Summary
Brief summary
This study looks at the feasibility of using Technitium, injected via a bronchoscope, for the detection of the sentinel lymph node in suspected non-small cell lung cancer Who is it for? You can join this study if you are: - about to undergo flexible bronchoscopy for the diagnosis of suspected non-small cell lung cancer - 40-85 years of age - prepared to accept the 2% risk of developing a pneumothorax (collapsed lung) with this treatment. Trial details While having their scheduled bronchoscope, participants will receive injection of technetium dye into the region of the lung which has the lung cancer. The technetium will allow any sentinel lymph nodes to be identified by a non-invasive Nuclear Medicine imaging test called a SPECT/CT scans, 4 hours after the injection. The study will look at the effectiveness and safety of this procedure.
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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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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Daniel Steinfort
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Address
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c/- Dept Respiratory Medicine
Royal Melbourne Hospital
Grattan St
Parkville
Victoria 3050
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Country
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Australia
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Phone
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+61 3 9342 7708
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Fax
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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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Dr Daniel Steinfort
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Address
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c/- Dept Respiratory Medicine
Royal Melbourne Hospital
Grattan St
Parkville
Victoria 3050
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Country
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Australia
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Phone
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+61 3 9342 7708
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Fax
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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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