A randomized, controlled clinical trial of the homeopathic medication TRAUMEEL s® in the treatment of chemotherapy-induced stomatitis in children undergoing stem cell transplantation
Menachem Oberbaum, M.D. 1 *, Isaac Yaniv, M.D. 2, Yael Ben-Gal, R.N. 2, Jerry Stein, M.D. 2, Nurit Ben-Zvi, R.N. 2, Laurence S. Freedman, Ph.D. 3, David Branski, M.D. 4
1The Institute of Research on Complementary Medicine, The Center of Integrated Complementary Medicine, Shaare Zedek Medical Center, Jerusalem, Israel
2Bone Marrow Transplantation Unit, The Schneider Children's Medical Center of Israel, Rabin Medical Center, Petach Tikva, Sackler School of Medicine, Tel-Aviv University, Israel
3Department of Mathematics, Statistics, and Computer Sciences, Bar-Ilan University. Ramat-Gan, Israel
4Department of Pediatrics, Shaare Zedek Medical Center, Hebrew University Medical School, Jerusalem, Israel
email: Menachem Oberbaum (
oberbaum@netvision.net.il)
*Correspondence to Menachem Oberbaum, The Institute of Research on Complementary Medicine, The Center of Integrated Complementary Medicine, Shaare Zedek Medical Center, P.O. Box 3235, Jerusalem 91031, Israel
Fax: +972-2-6666975
Funded by:
International Society of Homotoxicology, Baden-Baden, Germany
Keywords
TRAUMEEL S®; stomatitis; mucositis; autologous; allogeneic; stem cell transplantation; bone marrow transplantation; randomized; placebo-controlled; homeopathy; complementary medicine
Abstract
BACKGROUND
Stomatitis is a common consequence of chemotherapy and a condition for which there is little effective treatment. Although the management of patients with other chemotherapy-related toxicities has improved in recent years, the incidence of stomatitis is increasing because of more intensive treatment and is often a dose limiting factor in chemotherapy. The authors assessed the efficacy of a homeopathic remedy, TRAUMEEL S®, in the management of chemotherapy-induced stomatitis in children undergoing bone marrow transplantation.
METHODS
A randomized, placebo-controlled, double-blind clinical trial was conducted in 32 patients ages 3-25 years who had undergone allogeneic (16 patients) or autologous (16 patients) stem cell transplantation. Of the 30 evaluable patients, 15 were assigned placebo, and 15 were assigned TRAUMEEL S both as a mouth rinse, administered five times daily from 2 days after transplantation for a minimum of 14 days, or until at least 2 days after all signs of stomatitis were absent. Stomatitis scores were evaluated according to the World Health Organization grading system for mucositis.
RESULTS
A total of five patients (33%) in the TRAUMEEL S treatment group did not develop stomatitis compared with only one patient (7%) in the placebo group. Stomatitis worsened in only 7 patients (47%) in the TRAUMEEL S treatment group compared with 14 patients (93%) in the placebo group. The mean area under the curve stomatitis scores were 10.4 in the TRAUMEEL S treatment group and 24.3 in the placebo group. This difference was statistically significant (P < 0.01).
CONCLUSIONS
This study indicates that TRAUMEEL S may reduce significantly the severity and duration of chemotherapy-induced stomatitis in children undergoing bone marrow transplantation. Cancer 2001;92:684-90. © 2001 American Cancer Society.
Received: 21 December 2000; Revised: 27 March 2001; Accepted: 9 April 2001