None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age 18 years or older, histologically or cytologically documented cancer, radiologically diagnosed metastatic cancer 2) Complain of more than 4 points when we evaluate the grade of anorexia using Visual Analogue Scale(VAS) 3) Eastern Cooperative Oncology Group (ECOG) performance status =2 4) People who volunteered to participate in this clinical study and signed the informed consent
Exclusion criteria
Exclusion criteria: 1) People who intend to receive chemotherapy or radiotherapy during the study period 2) People who have received chemotherapy or radiotherapy in the 4 weeks prior to the study 3) People who have local skin problems at or near the moxibution sites 4) People who have impossible oral intake, severe insomnia or depression 5) People who have diseases which can influence on appetite (such as hypoadrenalism, etc) 6) People who are receiving appetizers (such as megestrol acetate, corticosteroids, etc) 7) Others who are judged to be difficult to perform the clinical study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the change of anorexia cachexia subscale(ACS) score among FAACT | — |
Secondary
| Measure | Time frame |
|---|---|
| the change of other scores besides anorexia cachexia subscale(ACS) among FAACT ;the change of WORTC QLQ-C30 scores;the change of anorexia VAS score ;the change of WBC value;the change of neutrophil value;the change of platelet value;the change of CRP value;the change of fibrinogen value | — |
Countries
Korea, Republic of
Contacts
Daejeon Korean Medicine Hospital of Daejeon University