1. A Double-Blind, Randomized, Placebo-Controlled Trial ofPanax Ginsengfor Cancer-Related Fatigue in Patients With Advanced Cancer
- Author
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Lorenzo Cohen, Helen L. House, Zhanni Lu, Ahsan Azhar, Sriram Yennurajalingam, Akhila Reddy, Angelique Wong, Deborah A. Kuban, Zita Dubauskas Lim, Sunil M. Patel, Eduardo Bruera, Kenneth R. Hess, Janet L. Williams, Gabriel Lopez, Ahmed Kaseb, Susan Frisbee-Hume, Kyu Hyoung Lim, and Nizar M. Tannir
- Subjects
0301 basic medicine ,medicine.medical_specialty ,business.industry ,Placebo-controlled study ,Hospital Anxiety and Depression Scale ,Placebo ,law.invention ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Mood ,Oncology ,Randomized controlled trial ,law ,030220 oncology & carcinogenesis ,Internal medicine ,Clinical endpoint ,Medicine ,Anxiety ,medicine.symptom ,business ,Cancer-related fatigue - Abstract
Background: Despite the high frequency, severity, and effects of cancer-related fatigue (CRF) on the quality of life (QoL) of patients with cancer, limited treatment options are available. The primary objective of this study was to compare the effects of oral Panax ginseng extract (PG) and placebo on CRF. Secondary objectives were to determine the effects of PG on QoL, mood, and function. Methods: In this randomized, double-blind, placebo-controlled study, patients with CRF ≥4/10 on the Edmonton Symptom Assessment System (ESAS) were eligible. Based on a pilot study, we randomized patients to receive either 400 mg of standardized PG twice daily or a matching placebo for 28 days. The primary end point was change in the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) subscale from baseline to day 29. Results: Of 127 patients, 112 (88.2%) were evaluable. The mean (SD) FACIT-F subscale scores at baseline, day 15, and day 29 were 22.4 (10.1), 29.9 (10.6), and 30.1 (11.6) for PG (P
- Published
- 2017
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