4.6 Article

Phase II trial of encapsulated ginger as a treatment for chemotherapy-induced nausea and vomiting

Journal

SUPPORTIVE CARE IN CANCER
Volume 17, Issue 5, Pages 563-572

Publisher

SPRINGER
DOI: 10.1007/s00520-008-0528-8

Keywords

Ginger; Apripetant; Chemotherapy-induced nausea and vomiting

Funding

  1. National Center for Complementary and Alternative Medicine (NCCAM) [1 KO7 CA102592-01, R21AT0001735]
  2. [NCI CN-55124]
  3. [NCI U10CA74648]
  4. DIVISION OF CANCER PREVENTION AND CONTROL [N01CN055124] Funding Source: NIH RePORTER
  5. NATIONAL CANCER INSTITUTE [K07CA102592, U10CA074648] Funding Source: NIH RePORTER
  6. NATIONAL CENTER FOR COMPLEMENTARY &ALTERNATIVE MEDICINE [R21AT001735] Funding Source: NIH RePORTER
  7. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000042] Funding Source: NIH RePORTER

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Ginger has been used to treat numerous types of nausea and vomiting. Ginger has also been studied for its efficacy for acute chemotherapy-induced nausea and vomiting (CINV). However, its efficacy for delayed CINV in a diverse oncology population is unknown. We performed a randomized, double-blind, placebo-controlled trial in 162 patients with cancer who were receiving chemotherapy and had experienced CINV during at least one previous round of chemotherapy. All participants were receiving a 5-HT3 receptor antagonists and/or aprepitant. Participants were randomized to receive either 1.0 g ginger, 2.0 g ginger daily, or matching placebo for 3 days. The primary outcome was change in the prevalence of delayed CINV. Secondary outcomes included acute prevalence of CINV, acute and delayed severity of CINV, and assessment of blinding. There were no differences between groups in the prevalence of delayed nausea or vomiting, prevalence of acute CINV, or severity of delayed vomiting or acute nausea and vomiting. Participants who took both ginger and aprepitant had more severe acute nausea than participants who took only aprepitant. Participants were able to accurately guess which treatment they had received. Ginger appeared well tolerated, with no difference in all adverse events (AEs) and significantly less fatigue and miscellaneous AEs in the ginger group. Ginger provides no additional benefit for reduction of the prevalence or severity of acute or delayed CINV when given with 5-HT3 receptor antagonists and/or aprepitant.

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