gastric cancer
Conditions
Interventions
None listed
Sponsors
Hiroshima Prefectural Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Cases undergoing gastric cancer surgery Cases in which test results and other clinical data can be provided to the research office for this study Cases in which consent can be obtained from the patient's blood relative, parent, spouse, or guardian in cases involving minors or adults who lack the capacity to consent.
Exclusion criteria
Exclusion criteria: Patients who have not given consent Patients who the responsible researcher or attending physician deems inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 6-minute walk test at the first consultation, preoperatively (at the time of hospitalization for surgery), at the time of discharge, 1 week, 4 weeks, and 12 weeks after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| test data (blood count, biochemistry), body composition, grip strength, leg circumference, Bathel index, motor function evaluation (short physical performance battery) at the first consultation, preoperatively (at the time of hospitalization for surgery), at the time of discharge, 1 week, 4 weeks, and 12 weeks after surgery. | — |
Countries
Japan
Contacts
Public ContactNobuaki Fujikuni
Hiroshima Prefectural Hospital Department of Gastroenterological Surgery
Outcome results
None listed