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1. induction therapy adverse events AML NCT00180102

- 20/09/2021 - 1 Formulário, 49 Grupos de itens, 239 Elementos de dados, 2 Idiomas
Grupos de itens: General information, allergic reaction, Hämoglobin, Leukocytes, Neutrophils, Platelets, Arrhythmias, Cardiac ischemia/infarction, Hypertension, Hypotension, Left ventricular systolic dysfunction, Pericarditis, Pulmonary Hypertension, DIC, Fibrinogen, Fever (Neutrophils > 1,0 GPt/l), Neutropenic fever, Rash/desquamation, Pancreas endocrine, Diarrhea, Dysphagia/Esophagitis/Gastritis/Ileus, Enteritis, Mukositis/Stomatitis, Nausea and vomiting, Hemorrhage, Pankreatitis, Infection, Alkaline Phosphatase, ALAT, GPT, ASAT, GOT, Bilirubin, Creatinine, GGT, Ataxia, Motor neuropathy, Sensory neuropathy, Seizures, Nystagmus, Disorder of eye, Pain, Dyspnea, Hypoxia, Pleural effusion (non-malignant), Pneumonitis/pulmonary infiltrates, Cystitis, Tumor lysis syndrome, Thrombosis and Embolism, other, Unterschrift
Randomisierter Vergleich zwischen Standard- und intensivierter Therapiestrategie der akuten myeloischen Leukämie des Erwachsenen im Alter von <= 60 Jahren Prospektive, randomisierte, multizentrische Therapieoptimierungsstudie - Studienprotokoll AML2003 http://www.clinicaltrials.gov/ct2/show/NCT00180102

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