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Trial registered on ANZCTR
Registration number
ACTRN12612000579897
Ethics application status
Approved
Date submitted
22/05/2012
Date registered
29/05/2012
Date last updated
24/01/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Early tube feeding in head and neck cancer
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Scientific title
A randomized comparison of early prophylactic feeding via gastrostomy versus standard care in high risk patients with head and neck cancer to determine impact on nutrition outcomes, quality of life and clinical outcomes
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Secondary ID [1]
280533
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Nil
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Universal Trial Number (UTN)
U1111-1131-0924
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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:
Head and neck cancer
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Malnutrition
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Condition category
Condition code
Cancer
286793
286793
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0
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Head and neck
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Diet and Nutrition
286794
286794
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0
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Other diet and nutrition disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Patients randomised to the intervention will commence two supplementary bolus feeds (standard enteral formula 1.5kcal/ml with fibre) per day in addition to usual dietary intake at the time of gastrostomy placement.
The supplementary feeds will continue pre treatment and throughout treatment. Most patients will be anticipated to be receiving chemoradiotherapy with a duration of 7 weeks. Tube placement is usually within 1-2 weeks prior to chemoradiotherapy, and so total predicted duration of intervention is 8-9 weeks.
Additional feeds will be commenced as clinically indicated during treatment by the clinical dietitian.
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Intervention code [1]
284908
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Treatment: Other
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Intervention code [2]
284964
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Prevention
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Comparator / control treatment
Patients randomised to standard care will commence water flushes via the gastrostomy at the time of gastrostomy placement and throughout treatment. Feeds will be commenced as clinically indicated throughout treatment as per current standard care.
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Control group
Active
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Outcomes
Primary outcome [1]
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Weight (to calculate % weight loss over time)
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Assessment method [1]
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Timepoint [1]
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baseline, 3 months post completion of primary treatment for head and neck cancer
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Secondary outcome [1]
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Body composition (BIA to measure fat free mass)
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Assessment method [1]
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Timepoint [1]
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baseline and 3 months post completion of primary treatment for head and neck cancer
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Secondary outcome [2]
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Nutritional status (Patient generated subjective global assessment)
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Assessment method [2]
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Timepoint [2]
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baseline and 3 months post completion of primary treatment for head and neck cancer
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Secondary outcome [3]
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Quality of life (EORTC QLQ-C30, EORTC H&N35)
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Assessment method [3]
297529
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Timepoint [3]
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baseline and 3 months post completion of primary treatment for head and neck cancer
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Eligibility
Key inclusion criteria
Diagnosed with head and neck cancer
AND
Referred for prophylactic gastrostomy prior to treatment
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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
patients with severe malnutrition at diagnosis
OR
patients with moderate malnutrition and severe dysphagia at diagnosis (requiring puree/liquid diets)
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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)
Patient identified by medical oncologist at pre treatment clinic and referred to research dietitian to determine final eligibility based on nutritional assessment. Research dietitian to complete recruitment and consent. Patient will then be randomised by independent researcher team member not involved with the intervention or data collection.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation method using computer generated random sequence numbers. Patients will also be stratified according to nutritional status.
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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
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/07/2012
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Actual
19/09/2012
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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
123
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
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Royal Brisbane & Womens Hospital - Herston
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Recruitment postcode(s) [1]
6227
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4029 - Royal Brisbane Hospital
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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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Royal Brisbane and Women's Hospital
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Address [1]
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Butterfield Street
Herston
QLD
4029
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Country [1]
285292
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Australia
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Primary sponsor type
Individual
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Name
Teresa Brown
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Address
Dept Nutrition and Dietetics, RBWH
Level 2 James Mayne Building
Butterfield Street
Herston
QLD
4029
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Judith Bauer
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Address [1]
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School of Human Movement Studies
University of Queensland
St Lucia
QLD
4072
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Country [1]
284151
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Australia
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Secondary sponsor category [2]
284152
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Individual
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Name [2]
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Merrilyn Banks
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Address [2]
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Dept Nutrition and Dietetics, RBWH
Level 2 James Mayne Building
Butterfield Street
Herston
QLD
4029
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Country [2]
284152
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Australia
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Secondary sponsor category [3]
284153
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Individual
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Name [3]
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Brett Hughes
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Address [3]
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Cancer Care Services, RBWH
Level 5 Joyce Twedell Building
Butterfield Street
Herston
QLD
4029
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Country [3]
284153
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Liz Kenny
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Address [1]
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Cancer Care Services, RBWH
Level 5 Joyce Twedell Building
Butterfield Street
Herston
QLD
4029
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Country [1]
260810
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Australia
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Other collaborator category [2]
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Individual
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Name [2]
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Charles Lin
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Address [2]
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Cancer Care Services, RBWH
Level 5 Joyce Twedell Building
Butterfield Street
Herston
QLD
4029
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Country [2]
260811
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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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Royal Brisbane and Womens Hospital
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Ethics committee address [1]
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Butterfield Street Herston QLD 4029
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Ethics committee country [1]
287305
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Australia
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Date submitted for ethics approval [1]
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29/05/2012
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Approval date [1]
287305
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Ethics approval number [1]
287305
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HREC/12/QRBW/162
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Ethics committee name [2]
288695
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The University of Queensland
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Ethics committee address [2]
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Cumbrae-Stewart Building Research Road Brisbane QLD 4072
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Ethics committee country [2]
288695
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Australia
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Date submitted for ethics approval [2]
288695
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Approval date [2]
288695
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Ethics approval number [2]
288695
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2012000890
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Summary
Brief summary
This study aims to compare the outcome of early tube feeding compared to commencement of feeding as per current standard practice in patients undergoing gastrostomy prior to treatment for head and neck cancer. Who is it for? You may be eligible to join this study if you are aged 18 years or above, have been diagnosed with head and neck cancer, and have been referred for a preventive gastrostomy (insertion of feeding tube into the stomach) prior to treatment for your cancer. Trial details Participants in this trial will be randomly (by chance) allocated to one of two treatment groups. Participants in one group will commence two supplementary feeds per day at the time of feeding tube insertion (gastrostomy). These feeds will be in addition to the patient's usual dietary intake and will continue throughout cancer treatment. Participants in the other group will receive standard care. This involves water flushes via the gastrostomy throughout cancer treatment and feeds will be commenced by the dietitian as clinically indicated during treatment. Participants will be assessed at baseline and 3 months post completion of treatment in order to determine impact on nutrition outcomes, quality of life and clinical outcomes.
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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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Ms Teresa Brown
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Address
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Nutrition & Dietetics
Level 2 James Mayne Buidling
Royal Brisbane & Womens Hospital
Butterfield Street, Herston
Qld 4029
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Country
34210
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Australia
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Phone
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+61 7 36467997
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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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Teresa Brown
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Address
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Dept Nutrition and Dietetics
Level 2 James Mayne Building, RBWH
Butterfield Street
Herston
QLD
4029
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Country
17457
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Australia
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Phone
17457
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+617 3646 7997
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Fax
17457
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+617 3646 1874
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Email
17457
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[email protected]
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Contact person for scientific queries
Name
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Teresa Brown
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Address
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Dept Nutrition and Dietetics
Level 2 James Mayne Building, RBWH
Butterfield Street
Herston
QLD
4029
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Country
8385
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Australia
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Phone
8385
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+617 3646 7997
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Fax
8385
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+617 3646 1874
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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
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Study results article
Yes
Publication Date - 23 May 2017 Brown, T., Banks...
[
More Details
]
362532-(Uploaded-07-01-2021-12-39-21)-Journal results publication.pdf
Study results article
Yes
Publication Date - 5 July 2017 Teresa Brown, Me...
[
More Details
]
362532-(Uploaded-07-01-2021-12-46-55)-Journal results publication.pdf
Study results article
Yes
Publication Date - 25 July 2017 Teresa Brown, M...
[
More Details
]
362532-(Uploaded-07-01-2021-12-49-50)-Journal results publication.pdf
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Impact of early prophylactic feeding on long term tube dependency outcomes in patients with head and neck cancer.
2017
https://dx.doi.org/10.1016/j.oraloncology.2017.06.025
Embase
Randomised controlled trial of early prophylactic feeding vs standard care in patients with head and neck cancer.
2017
https://dx.doi.org/10.1038/bjc.2017.138
Embase
Tube feeding during treatment for head and neck cancer - Adherence and patient reported barriers.
2017
https://dx.doi.org/10.1016/j.oraloncology.2017.07.017
Embase
Impact of sarcopenia and myosteatosis on survival outcomes for patients with head and neck cancer undergoing curative-intent treatment.
2023
https://dx.doi.org/10.1017/S0007114522000435
N.B. These documents automatically identified may not have been verified by the study sponsor.
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