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Effect of Yukgunja-tang for Anorexia in Cancer Patients

Effect of Yukgunja-tang for Anorexia in Cancer Patients : A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002847
Enrollment
52
Registered
2018-05-04
Start date
2018-04-03
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : KracieYookgoonjatang Extract Fine Granule (YGJT) Participants in YGJT group will be administered YGJT at a dose of 3g two times per day(total daily dose of 6.0g) for 4 weeks, total 56 times.

Sponsors

Dunsan Korean Medicine Hospital of Daejeon University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) patients who have a histologically or cytologically confirmed solid tumour; individuals who are suffering from anorexia 2) men and women aged 20-80 years who can write and understand 3) Visual analog scale(VAS) for anorexia = 40/100 mm 5) neutrophils =1500/µL, platelets =100,000/µL 6) total bilirubin of the maximum normal level or less (1.2 mg/dL) 7) alanine aminotransferase(ALT), aspartate aminotransferase(AST) lower than 2-fold the upper limit of normal (35/45U/l) 8) creatinine lower than 1.5 fold the upper limit of normal (1.09 mg/dL) 9) written informed consent for participation in the trial

Exclusion criteria

Exclusion criteria: 1) impossible to intake orally 2) Patients who are undergoing chemotherapy or less than one month after completion of chemotherapy 3) survived at least 5 years after cancer diagnosis (with no additional cancer diagnosis) 4) Eastern Cooperative Oncology Group (ECOG) performance status score = 3 5) Patients who have dementia, delirium or depression 6) reports more than 7 points of Numeric Pain Rating Scale in 2 weeks of screening 7) Patients who have diseases like hypoadrenalism which can influence on appetite 8) Patients who are taking appetite stimulants such as megestrol acetate, corticosteroids and thalidomide 9) Women of childbearing potential 10) others who are judged not to be appropriate to study

Design outcomes

Secondary

MeasureTime frame
The changes in Functional Assessment of Anorexia/Cachexia Therapy (FAACT) score (except Anorexia cachexia subscale);Cost per visual analog scale(VAS);Visual analog scale(VAS) for anoreixa;weight and body mass index(BMI);Leptin;Tumor necrosis factor a (TNF-a);Ghrelin;Interleukin-6(IL-6)

Primary

MeasureTime frame
The changes in the anorexia/ cachexia subscale of Functional Assessment of Anorexia/Cachexia Therapy (FAACT);cost per QALY(Quality Adjusted Life Years) gained

Countries

Korea, Republic of

Contacts

Public ContactMi kyung Jeong

Dunsan Korean Medicine Hospital of Daejeon University

oiny_2000@hanmail.net+82-42-470-9488

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 20, 2026