Total Body Composition in Detection of Nutrition Depletion in Head and Neck Patients
NCT ID: NCT02854735
Last Updated: 2016-08-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
120 participants
OBSERVATIONAL
2015-02-28
2018-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Head and neck neoplasm
Patients with stage III-IV head and neck cancer (squamous cell carcinoma) patient undergoing CCRT
Imaging by CT and densitometry
Imaging by CT and densitometry, no intervention involved
Interventions
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Imaging by CT and densitometry
Imaging by CT and densitometry, no intervention involved
Eligibility Criteria
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Inclusion Criteria
2. 2010 7th edition AJCC stage III, IVA (T4N0-2) and IVB (any T, N3).
3. Well-informed and accepted treatment of CCRT.
4. Age 20-70 years old.
5. Negative pregnancy test for women of childbearing potential.
6. Adequate hematopoietic or organ function which is amenable for chemotherapy:
* A leukocyte count ≥3000/L
* Platelet count ≥100,000/L.
* Serum bilirubin level ≦ 1.5mg/dL
* Serum creatinine level ≦1.6 mg/dL or creatinine clearance ≥ 60 mL/min/1.73 m2.
* ALT/AST ≦ 3X ULN
9\. Ability to understand and willingness to be enrolled in our study and sign a written informed consent document
Exclusion Criteria
2. Patients have acute medical conditions (such as bacterial or viral infection or active cardiopulmonary disease) that may be incapable of having regular image study.
3. Patients are under regular steroid or hyperthyroid medications, which may have great impact on the whole body metabolism.
4. Patients are under-nutrient and they need to have regular liquid oral nutrition formulas support.
5. Patient that have dementia or pregnant.
6. Patients not expecting to comply with follow up.
7. Patient not suitable for chemotherapy.
8. Patient not suitable for MRI, such as claustrophobia, previous metal implantation, previous cardiac pacemaker implantation, inability to comply with MRI instructions and poor renal function.
9. Received barium study within a week.
20 Years
70 Years
ALL
No
Sponsors
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Chang Gung Memorial Hospital
OTHER
Responsible Party
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Locations
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Chang Gung Memorial Hospital
Guishan, Taoyuan, Taiwan
Countries
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Facility Contacts
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Other Identifiers
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CMRPG2E0101
Identifier Type: -
Identifier Source: org_study_id
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