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Sipjeondaebo-tang in patients with cancer with anorexia: a protocol for a pilot, randomised, controlled trial
  1. Chunhoo Cheon1,
  2. Sunju Park2,
  3. Yu Lee Park1,
  4. Ching-Wen Huang1,
  5. Youme Ko1,
  6. Bo-Hyoung Jang1,
  7. Yong-Cheol Shin1,
  8. Seong-Gyu Ko1
  1. 1Department of Korean Preventive Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea
  2. 2Department of Preventive Medicine, College of Korean Medicine, Daejeon University, Daejeon, Republic of Korea
  1. Correspondence to Professor Seong-Gyu Ko; epiko{at}khu.ac.kr

Abstract

Introduction Cancer-related anorexia is the loss of appetite or desire to eat in patients with cancer. Although treatments for cancer-related anorexia do exist, patients have sought complementary and alternative medicine including herbal remedies, due to safety concerns. Sipjeondaebo-tang is one among other popular herbal medicines that are beneficial to management of anorexia in Korea. The purpose of this study is to examine the feasibility for a full randomised clinical trial of Sipjeondaebo-tang for cancer-related anorexia.

Methods and analysis This study is a randomised, double-blinded and placebo-controlled trial of Sipjeondaebo-tang. For the study, 40 patients with cancer, aged 20–80 years, who reported anorexia, will be recruited. The participants will receive either 3 g of Sipjeondaebo-tang or a placebo, 3 times a day for 4 weeks. The primary end point is a change in the anorexia/cachexia subscale (A/CS) of Functional Assessment of Anorexia/Cachexia Therapy (FAACT). The secondary end points include changes in the visual analogue scale (VAS) of appetite, cortisol and ghrelin. The outcomes will be measured on every visit. Each participant will visit once a week during 4 weeks.

Ethics and dissemination The present study has been approved by the Institutional Review Board of the Dunsan Korean Medicine Hospital of Daejeon University (reference DJDSKH-15-03-2 (V.2.0)). The results will be disseminated in a peer-reviewed journal and scientific conference.

Trial registration number NCT02468141; Pre-results.

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