Repeated CT study in patients with cervical cancer to assess organ motion for adaptive radiotherapy and proton therapy planning
Completed
- Conditions
- cervical cancercervical carcinoma10038594
- Registration Number
- NL-OMON42122
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
Patients with histologically proven cervical carcinoma
Radiotherapy as primary treatment, with or without concurrent chemotherapy
FIGO stage I, II, III
>=23 fractions of radiation therapy planned (curative schedule)
Age >=18 years
Written informed consent
Exclusion Criteria
FIGO stage IV
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>A strategy for adaptive proton radiotherapy to irradiate patients with a<br /><br>cervical carcinoma with protons in an accurate and safe way. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Developed and tested use of a plan library<br /><br>The amount of robustness in treatment planning still necessary </p><br>