Actively Recruiting
Long-term Neurovascular Complications After Radiation Therapy in Head and Neck Cancer
Led by Chang Gung Memorial Hospital · Updated on 2026-03-20
800
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Head and neck cancer is a group of cancers develop from the soft tissues, salivary gland, mucosa of the upper respiratory or digestive system covering the oral and nasal cavity. Radiotherapy is usually the standard treatment of Head and neck cancers. In the present study, investigators aim to study the prevalence of cervical-cranial vascular complications during the early stages in these Head and neck cancer patients receiving Radiotherapy. Investigators will also compare the results between Nasopharyngeal cancer and other Head and neck cancerpatients receiving Radiotherapy.
CONDITIONS
Official Title
Long-term Neurovascular Complications After Radiation Therapy in Head and Neck Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 20 years or older
- Diagnosed with head and neck cancer
- Received radiation therapy within 72 months before joining the prospective cohort
- Had at least 1 brain image and cervical-cranial vascular study between end of radiation therapy and enrollment date (prospective cohort)
- Received radiation therapy more than 120 months before the IRB adoption date for the retrospective validation cohort
- Had at least 2 brain images and cervical-cranial vascular studies between end of radiation therapy and 6 to 10 years after, with one study within 5 years and another after 5 years post-radiation therapy (retrospective validation cohort)
You will not qualify if you...
- Younger than 20 years old
- Not willing to sign the informed consent form
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chang Gung Memorial Hospital
Taipei, Taiwan
Actively Recruiting
Research Team
C
Chi-Hung Liu
CONTACT
H
Hui-Ching Kang
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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