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Trial registered on ANZCTR
Registration number
ACTRN12616000877482
Ethics application status
Approved
Date submitted
27/06/2016
Date registered
5/07/2016
Date last updated
5/07/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Prospective Cohort Study to Assess Body Composition as a Predictor of Outcomes in Pancreatic Cancer
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Scientific title
A Prospective Cohort Study to Assess Body Composition as a Predictor of Outcomes in Pancreatic Ductal Adenocarcinoma
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Secondary ID [1]
289549
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Nil Known
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Universal Trial Number (UTN)
U1111-1184-7244
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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:
Pancreatic Ductal Adenocarcinoma
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Condition category
Condition code
Cancer
299274
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0
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Pancreatic
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
6
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Target follow-up type
Months
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Description of intervention(s) / exposure
This is an observational study, tracking muscle mass and strength during standard of care chemotherapy treatment. The muscle mass will be measured on standard of care CT scans. Muscle function will be assessed using grip strength measurement (1 minute) and peak expiratory flow measurement (2 minutes). An anorexia questionnaire will also be provided (2 minutes)
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Intervention code [1]
295145
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Chemotherapy toxicity (occurrence of adverse event gr3 or 4), assessed by review of medical records
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Assessment method [1]
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Timepoint [1]
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diagnosis, 3 months and 6 months
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Secondary outcome [1]
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Survival (by review of medical records)
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Assessment method [1]
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Timepoint [1]
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at diagnosis (baseline), 3 months 6 months
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Secondary outcome [2]
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Skeletal muscle volume (measured on standard of care CT scans)
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Assessment method [2]
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Timepoint [2]
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at diagnosis, 3 months & 6 months
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Secondary outcome [3]
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skeletal muscle strength (peak expiratory flow + handgrip strength)
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Assessment method [3]
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Timepoint [3]
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at diagnosis, 3 months and 6 months
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Secondary outcome [4]
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Anorexia as measured by the "Functional Assessment of Anorexia and Cachexia Therapy" questionnaire
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Assessment method [4]
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Timepoint [4]
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diagnosis, 3 months, 6 months
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Eligibility
Key inclusion criteria
-Adult
-Pancreatic ductal adenocarcinoma
-Diagnosed with pancreatic cancer within the last month
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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
Neuromuscular disease
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Number of participants required was determined using a power calculation, based on a similar study, which examined breast cancer patients on Capcitabine. This calculation was based of a power or 20%, and effect size of 30%, and a p value <0.05 required to be deemed statistically significant. All data will be analysed using GraphPad Prism 6 for Mac OS X (GraphPad Software, San Diego, CA, USA). Categorical data will be assessed for statistical significance using Chi square test. Continuous data will be tested for normality using D’Agostino & Pearson omnibus normality test. When only two groups of data are being compared the unpaired t-test or Mann-Whitney test will used. The unpaired t-test, with Welch’s correction to allow for comparison of groups with different standard deviations, will be used for data with Gaussian distribution (parametric data), and the Mann-Whitney test will be used for analysis of non-parametric data. When there are more than two groups being compared the ordinary one-way analysis of variance (ANOVA) and Kruskal-Wallis ANOVA will be used. Parametric data was analysed using an ordinary one-way ANOVA and non-parametric data will be analysed using the Kruskal-Wallis ANOVA. When a significant result was determined from either ANOVA test, the unpaired t-test or Mann-Whitney test was used, depending of distribution of the data, to compare each of the groups. For all analysis, a p value of <0.05 was considered significant.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
1/03/2016
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Date of last participant enrolment
Anticipated
22/02/2017
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Actual
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Date of last data collection
Anticipated
7/04/2017
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Actual
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Sample size
Target
90
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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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Recruitment hospital [1]
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [2]
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Cabrini Hospital - Malvern - Malvern
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Recruitment postcode(s) [1]
13476
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3144 - Malvern
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Recruitment postcode(s) [2]
13477
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3168 - Clayton
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Monash Medical Centre
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Address [1]
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Department of Gastroenterology
Monash Medical Centre
246 Clayton Rd
Clayton, Vic
3168
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
Monash Health
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Address
246 Clayton road
Clayton, Vic
3168
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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Monash University
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Address [1]
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Wellington Rd & Blackburn Rd, Clayton VIC 3800
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Country [1]
292747
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Monash Health Low Risk Human Ethics Comittee
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Ethics committee address [1]
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246 Clayton Rd Clayton, Vic 3168
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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05/02/2016
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Approval date [1]
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25/02/2016
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Ethics approval number [1]
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LNR/16/MonH/27
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Summary
Brief summary
The primary purpose of this trial is to evaluate the link between body composition and outcomes in pancreatic cancer. Who is it for? You may be eligible to participate in this study if you are aged 18 or over and have been diagnosed with pancreatic ductal adenocarcinoma within the last month. Study details All participants enrolled in this study will complete a number of assessments including hand grip strength testing, a questionnaire and lung function tests at enrolment and 3 and 6 months later. The researchers will also require access to CT scans which have been collected as a part of your cancer management. It is hoped that the findings from this study will inform researchers on the links between muscle mass and function, and cancer outcomes of chemotherapy toxicity and survival.
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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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Dr Gregory Moore
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Address
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Department of Gastroenterology
Monash Medical Centre
246 Clayton Rd
Clayton, Vic
3168
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Country
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Australia
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Phone
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+61395946666
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Julia Freckelton
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Address
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Department of Gastroenterology
Monash Medical Centre
246 Clayton Rd
Clayton, Vic
3168
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Country
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Australia
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Phone
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+61395946666
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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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Julia Freckelton
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Address
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Department of Gastroenterology
Monash Medical Centre
246 Clayton Rd
Clayton, Vic
3168
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Country
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Australia
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Phone
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+61395946666
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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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