Concurrent, daily-low-dose cisplatin-based chemoradiation in patients with cervical cancer, Exploratory Trial
Not Applicable
- Conditions
- cervical cancer
- Registration Number
- JPRN-UMIN000024368
- Lead Sponsor
- Chiba University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 65
Inclusion Criteria
Not provided
Exclusion Criteria
1) positive para aortic lymph node swelling 2) severe systemic or uncontrolled disease (uncontrolled diabetes mellitus or hypertension) 3) severe infection that precluded the use of chemotherapy 4) preexisting neuropathy from any cause, pregnancy or lactation 5) mental illness 6) previous or concomitant malignancies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Overall survival
- Secondary Outcome Measures
Name Time Method Overall survival by histology Overall survival by age Adverse effects