Cervical cancer
Conditions
Interventions
None listed
Sponsors
Kagawa University Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1) Scheduled definitive treatment using IMRT for cervical cancer 2) 20 years old or older 3) Informed consent has been obtained
Exclusion criteria
Exclusion criteria: 1) Informed consent has not been obtained 2) Inappropriate patient for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IMRT completion rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy: overall survival, progression-free survival, locoregional control interval Safety: incidence of adverse event | — |
Countries
Japan
Contacts
Public ContactMasahide Anada
Kagawa University Hospital Department of Radiation Oncology
Outcome results
None listed