HFSR
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. in the clinical chemotherapy regimen; 2. patients were selected oral capecitabine with grade III hand foot syndrome in primary school and above, with a clear thinking, normal spirit, and a certain ability to understand and express; 3. volunteered to participate in the study and signed "informed consent".
Exclusion criteria
Exclusion criteria: 1. Patients who were allergic to the composition of self-made alveolar fluid; 2. the history of mental illness or the history of mental illness or mental illness; 3. no legal ability / limited capacity of behavior; 4. hindering the subjects to complete the study or sign of the medical or psychological status of the informed consent; 5. participating in other psychological studies and physiological experiments; 6. There are any researchers who may decide to compromise the coexistence of medical conditions or diseases in this study; 7.Patients with incomplete data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Grading of hand and foot reaction; | — |
Countries
China
Contacts
Cancer Center,Union Hospital, Tongji Medical College, Huazhong University of Science and Technology