Prospective interventional study on safety of carbon ion radiotherapy and image-guided brachytherapy for locally advanced uterine cervical cancer (GUNMA1202)
Not Applicable
- Conditions
- ocally advanced uterine cervical cancer
- Registration Number
- JPRN-UMIN000013340
- Lead Sponsor
- Gunma University Heavy Ion Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Female
- Target Recruitment
- 6
Inclusion Criteria
Not provided
Exclusion Criteria
1) Tumor invasion to gastro-intestinal tract. 2) Past history of chemotherapy. 3) Past history of radiotherapy in pelvis. 4) Uncontrolled infection in pelvis. 5) Severe concomitant diseases. 6) Active concurrent cancers. 7) (Possibly) pregnant patients. 8) Other medically or psychologically unsuitable circumstances are present.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Incidence of dose-limiting toxicity. 2) Incidence rate of acute adverse effects (within 90 days after the start of treatment).
- Secondary Outcome Measures
Name Time Method 1) Primary response in pelvis. 2) Incidence rate of late adverse effect (after 90 days from the start of treatment).