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Eur J Cancer ; 26 Suppl 1: S23-7, 1990.
Artigo em Inglês | MEDLINE | ID: mdl-2169782

RESUMO

A single-centre, double-blind, placebo-controlled study was carried out in 28 patients with malignant disease, naive to chemotherapy, receiving cisplatin at a mean dose in excess of 80 mg/m2. Patients were randomized into two groups, receiving either granisetron (40 micrograms/kg) or placebo. Patients in both groups who experienced symptoms of vomiting and nausea were given up to a further three 40 micrograms/kg doses of granisetron on an open-label basis, allowing the assessment of granisetron as an intervention anti-emetic in the placebo group. Following granisetron administration, 13 (93%) patients had no vomiting or nausea in the first 24 h, a significant difference compared with the one patient in the placebo group who remained free from vomiting and had only mild nausea in the same period (P less than 0.001). As a single intervention agent, granisetron achieved control or improvement of existing symptoms in the remaining members of the placebo group.


Assuntos
Cisplatino/efeitos adversos , Indazóis/uso terapêutico , Antagonistas da Serotonina/uso terapêutico , Vômito/prevenção & controle , Adulto , Idoso , Método Duplo-Cego , Feminino , Granisetron , Humanos , Masculino , Pessoa de Meia-Idade , Náusea/prevenção & controle , Neoplasias/tratamento farmacológico , Fatores Sexuais , Fatores de Tempo , Vômito/induzido quimicamente
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