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Trial registered on ANZCTR
Registration number
ACTRN12620000173998p
Ethics application status
Submitted, not yet approved
Date submitted
10/11/2019
Date registered
17/02/2020
Date last updated
17/02/2020
Date data sharing statement initially provided
17/02/2020
Type of registration
Prospectively registered
Titles & IDs
Public title
Tongue Reconstruction with Innervated Thigh Muscle
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Scientific title
Tongue Reconstruction with Innervated Vastus Lateralis and Antero-Lateral Thigh Free Flap
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Secondary ID [1]
299725
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Nil known
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Universal Trial Number (UTN)
N/A
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Trial acronym
TRIVALT
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Linked study record
N/A
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Health condition
Health condition(s) or problem(s) studied:
Tongue cancer
315072
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Condition category
Condition code
Cancer
313408
313408
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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
Reconstruction of defect following resection of tongue for malignancy with innervated vastus laterals and anterolateral thigh flap. The steps of this surgery are harvesting of the soft tissue flap and muscle with the innervation intact from the thigh, as routinely done for microvascular reconstruction of he tongue. Microvascular anastomosis will performed as per standard technique with 8-0 nylon. Surgery will be performed by Jonathan Clark/James Wykes. The duration of surgery will be on average 8-10 hours
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Intervention code [1]
315990
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Treatment: Surgery
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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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Assessment of the impact of innervated free flap reconstruction of large tongue defects after subtotal/total glossectomy on swallowing function (composite outcome)
The swallowing assessment is through videofluouroscopy, and functional endoscopic evaluation of swallowing
The speech assessment is through speech and intelligibility assessment (sentences from Frenchay Articulation Assessment, Rainbow Passage and Conversational Speech), intelligibility and percentage of consonants correct and subjective intelligibility by listeners blinded to patient characteristics, and speech handicap index (SHI)
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Assessment method [1]
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Timepoint [1]
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12 months after surgery
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Secondary outcome [1]
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Assessment of the impact of innervated free flap reconstruction of large tongue defects after subtotal/total glossectomy on speech function (composite outcome)
The swallowing assessment is through videofluouroscopy, and functional endoscopic evaluation of swallowing
The speech assessment is through speech and intelligibility assessment (sentences from Frenchay Articulation Assessment, Rainbow Passage and Conversational Speech), intelligibility and percentage of consonants correct and subjective intelligibility by listeners blinded to patient characteristics, and speech handicap index (SHI)
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Assessment method [1]
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Timepoint [1]
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12 months after surgery
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Secondary outcome [2]
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- To assess the impact of the intervention on Quality of Life (QoL) using EORTC H&N 35 questionnaire
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Assessment method [2]
377848
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Timepoint [2]
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12 months after surgery
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Secondary outcome [3]
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- To assess the impact of the intervention on tongue range of motion (using weighted scales 0-5 of each individual action, such as elevation, depression, right deviation, left deviation, protrusion, retraction)
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Assessment method [3]
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Timepoint [3]
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12 months after surgery
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Secondary outcome [4]
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- To assess the impact of innervated free flap reconstruction of the tongue on long-term airway patency and protection from aspiration using videofluroscopy and FEES (this is a composite score)
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Assessment method [4]
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Timepoint [4]
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12 months after surgery
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Eligibility
Key inclusion criteria
Tongue cancer requiring resection of >1/2 of the tongue
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Minimum age
18
Years
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Maximum age
80
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
- Preservation of the entire hypoglossal nerve on either side of the resection
- Contraindication for general anaesthesia
- Congenital or acquired neuro-degenerative disorder
- Inability to understand the study requirements or rehabilitation
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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)
Not applicable
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Not applicable
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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
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Descriptive statistics of analysis of speech, swallowing and sensorimotor function of tongue
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/03/2020
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Actual
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Date of last participant enrolment
Anticipated
31/12/2023
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Actual
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Date of last data collection
Anticipated
31/12/2024
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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)
NSW
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Recruitment hospital [1]
15106
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The Chris O’Brien Lifehouse - Camperdown
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Recruitment hospital [2]
15107
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Wollongong Hospital - Wollongong
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Recruitment postcode(s) [1]
28401
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2050 - Camperdown
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Recruitment postcode(s) [2]
28402
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2500 - Wollongong
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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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Chris O'Brien Lifehouse Hospital
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Address [1]
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119-143 Missenden Road, Camperdown NSW 2050
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Country [1]
304196
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Australia
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Primary sponsor type
Hospital
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Name
Chris O Brien Lifehouse Hospital
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Address
119-143 Missenden Road, Camperdown NSW 2050
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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]
304772
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Address [1]
304772
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Country [1]
304772
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
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Sydney Local Health District
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Ethics committee address [1]
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Level 11, KGV Building Missenden Road CAMPERDOWN NSW 2050
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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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30/09/2019
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Approval date [1]
304665
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Ethics approval number [1]
304665
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2019/ETH12967
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Summary
Brief summary
The purpose of this study is to trial a new method for rebuilding the tongue after cancer surgery Who is it for? You may be eligible for this study if you are aged 18 or over and have tongue cancer which requires at least half the tongue to be removed. Study details All participants in the study will undergo a reconstructive surgery where a piece of thigh muscle will be used to rebuild part of the tongue. This procedure takes place general anaesthesia during the same surgical procedure where the excision of the tongue cancer takes place, and the entire proceduretakes approximately 8-10 hours. As part of the study, all participants will have post-op assessments of tongue function and answer some questionnaires. It is hoped this study will help us better understand and standardize tongue reconstruction to improve speech and swallowing 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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Dr James Wykes
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Address
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VWO, Department of Surgery,
Wollongong Public Hospital,
Loftus St, Wollongong NSW 2500, Australia
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Country
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Australia
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Phone
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+61 410594383
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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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James Wykes
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Address
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VWO, Department of Surgery,
Wollongong Public Hospital,
Loftus St, Wollongong NSW 2500, Australia
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Country
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Australia
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Phone
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+61 410594383
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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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James Wykes
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Address
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VWO, Department of Surgery,
Wollongong Public Hospital,
Loftus St, Wollongong NSW 2500, Australia
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Country
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Australia
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Phone
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+61 410594383
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Fax
97780
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
For confidentiality reasons we do not plan to share IPD
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
5602
Study protocol
378680-(Uploaded-10-11-2019-12-59-53)-Study-related document.doc
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.
Download to PDF