None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Among the thyroid cancer patients suffering from the Radioactive-Iodine Induced Anorexia, people who got the therapy before 14 to 60 days, and complain of more than 4 points when we evaluate the grade of anorexia using Visual Analogue Scale(VAS) 2) People who are literate, 20-65 year old 3) People who volunteered to participate in this clinical study and signed the informed consent
Exclusion criteria
Exclusion criteria: 1) People who have impossible oral intake 2) People who are diagnosed and being treated with mental disease such as Dementia, Delirium, Depression, etc 3) People who complain of more than 7 points when we use Numeric Rating Scale, which can affect appetite or calorie intake, within 2 weeks of Clinical study screening 4) People who have diseases which can influence on appetite (such as hypoadrenalism, etc) 5) People who are receiving appetizers (such as megestrol acetate, corticosteroids, thalidomide) 6) Women who have the possibility of pregnancy 7) People who are beyond the Eastern Cooperative Oncology Group(ECOG) 2 8) Others who are judged to be difficult to perform the clinical study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anorexia Cachexia Subscale (ACS) score change among FAACT scale | — |
Secondary
| Measure | Time frame |
|---|---|
| Anorexia Cachexia Subscale (ACS) score change among FAACT scale ;other item score changes besides Anorexia Cachexia Subscale (ACS) among FAACT scale ;Anorexia VAS score change;Weight change;BMI change;ACTH, Cortisol numerical value change | — |
Countries
Korea, Republic of
Contacts
Daejeon Korean Medicine Hospital of Daejeon University