Solid cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.At least 18 years old at the time of obtaining consent 2.Cancer patients scheduled for or receiving systemic chemotherapy 3.Possible to visit research partner institutions that conduct blood sampling in advance 4.Can answer surveys 5.The principal investigator or research associate can determine that the investigator or research associate has the ability to understand and comply with the content of the clinical research 6.Able to sign and date ICF prior to enrollment in this study
Exclusion criteria
Exclusion criteria: 1.Patients receiving oral anticancer drugs only or hospitalized and not scheduled to use an outpatient chemotherapy unit 2.The principal investigator or principal research scientist determines that the subject is inappropriate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Waiting time1 Time spent at the collaborating institution for preliminary blood test and waiting time from the start of reception to the start of consultation on the day of chemotherapy at the implementing institution. Waiting time2 Waiting time from the start of reception to the start of consultation on the day of chemotherapy at the implementing medical institution when blood test are not taken in advance. | — |
Countries
Japan
Contacts
St. Marianna University School of Medicine Department of Clinical Oncology