Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1995 Sep;73(3):243-5.
doi: 10.1136/adc.73.3.243.

Randomised comparison of ondansetron and metoclopramide plus dexamethasone for chemotherapy induced emesis

Affiliations
Clinical Trial

Randomised comparison of ondansetron and metoclopramide plus dexamethasone for chemotherapy induced emesis

G S Dick et al. Arch Dis Child. 1995 Sep.

Abstract

The serotonin (5HT3) antagonist ondansetron was compared in a randomised study with metoclopramide and dexamethasone for the prevention of chemotherapy induced emesis. Thirty children aged 1-15 years with acute lymphoblastic leukaemia received 'intensification modules' according to the MRC United Kingdom acute lymphoblastic leukaemia regimen UKALL XI. This contains the moderately emetogenic drugs daunorubicin, etoposide, and cytarabine. Fifteen children received an intravenous loading dose of ondansetron followed by intravenous or oral doses 12 hourly for five days. Fifteen children received intravenous metoclopramide every six hours for three days with a loading dose of dexamethasone, repeated every eight hours for three days intravenously or orally. Efficacy was assessed by a diary card documenting the incidence of nausea, retching, or vomiting. In the 24 hour period after starting chemotherapy, ondansetron was more effective, with a complete or major response rate of 93%, compared with 33% using metoclopramide/dexamethasone.

PubMed Disclaimer

Similar articles

Cited by

References

    1. N Engl J Med. 1981 Oct 15;305(16):905-9 - PubMed
    1. Eur J Cancer Clin Oncol. 1983 Feb;19(2):203-8 - PubMed
    1. J Pediatr. 1984 Jan;104(1):138-40 - PubMed
    1. J Clin Oncol. 1985 Aug;3(8):1136-41 - PubMed
    1. Br Med J (Clin Res Ed). 1985 Oct 5;291(6500):930-2 - PubMed

Publication types

MeSH terms