ELEVATE study
- Conditions
- oropharynx cancer or hypopharynx cancerhead and neck cancer, opharynx cancer, hypopharynx cancerD006258
- Registration Number
- JPRN-jRCTs052220011
- Lead Sponsor
- emura Hirokazu
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
1. Patients with oropharynx or hypopharynx cancer (regardless of tissue system) who undergo chemoradiation treatment or radiation treatment as the first curative treatment. But, patients who have undergone chemotherapy prior to chemoradiation treatment or radiation treatment are included.
2. Age: 18 to 85 years old
3. Performance Status (ECOG) is 0 or 1 (within one month prior to obtaining consent)
4. Patients with written consent for participation of this clinical study from the patient or its representative
1. Patients whose don't recognize measurer's instructions (e.g. patients with dementia, aphasia, aphasia, higher brain dysfunction, intellectually disabled, etc.)
2. Patients who can't grip the tongue pressure probe with the front teeth (e.g. patients who are toothless jaws and are not wearing dentures)
3. Patients who can't crush the tongue pressure probe (e.., patients who cannot move the tongue at all)
4. Patients with dysphagia du to the pretreatment for head and neck cancer
5. Patients with significant decrease in swallowing function due to a history of central diseases, etc.
6. Other patients who are judged inadequate to this research by the principal (sub) investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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