A prospective observational study using ePRO-based symptom monitoring in patients with gynecologic and breast cancer
Not Applicable
- Conditions
- Gynecologic Cancer, Breast Cancer
- Registration Number
- JPRN-UMIN000050935
- Lead Sponsor
- ational Cancer Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients receiving cancer treatment for Synchronous cancers 2.Patients with treatment-emergent adverse events that have not resolved to baseline or Grade <= 2 according to CTCAE version 5.0. 3.Deemed otherwise unsuitable for the study by the principal investigator or other investigators
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method