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Keywords
Leucemia mieloide acuta M1 ×
- Clinical Trial (154)
- Eligibility Determination (110)
- Treatment Form (26)
- AML (24)
- Hematology (4)
- Follow-Up Studies (3)
- Laboratories (3)
- Leukemia (3)
- Stem Cell Transplantation (2)
- Off-Treatment (2)
- Pathology (2)
- Quality of Life (1)
- Ribavirin (1)
- Leukemia, Lymphocytic, Chronic, B-Cell (1)
- Bone Marrow Transplantation (1)
- Clinical Trial, Phase III (1)
- Peripheral Blood Stem Cell Transplantation (1)
- On-Study Form (1)
- Daunorubicin (1)
- Hematologic Tests (1)
- Myelodysplastic Syndromes (1)
Sommario
Modelli di dati selezionati
Devi effettuare il log in per selezionare i modelli di dati da scaricare per successive analisi
154 Risultati di ricerca.
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: CRF Header, AML: Form Administration, AML: Disease Description, Comments
Itemgroups: Adverse Events, Adverse Events specification, Death Sheet, Comments
Visit 1 - Medical History
6 itemgroups 47 elementiVisit Registration/Randomization I
5 itemgroups 20 elementiVisit 13 (End of Study)
20 itemgroups 182 elementiDrop out Sheet and visit
15 itemgroups 90 elementiVisit 7 (Day 15 Induction I)
10 itemgroups 87 elementiVisit 8 (before Day 1 Induction II)
9 itemgroups 123 elementi ItemGroup: Cytogenetics
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Header Module, On Treatment Report Period, Data amendment, Assessment Date, Mini Mental Examination Section, GDS, ADL, MOS Social Support Survey - Emotional/Informational Support, MOS Social Support Survey - Tangible support, Comorbidity Questionnaire, Comorbidity Questionnaire1, Medications/Sexual Function, Weight
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: ECOG clinical trial administrative data, Vital Status, Transplant Conditioning Regimen, Donor Information, Allogeneic Transplant, Transfusions, Comments, CCRR MODULE
Itemgroups: Header module, Record the highest grade of toxicity diagnosed since the previous evaluation. If this is the first evaluation, record the highest toxicity diagnosed since day 0. The toxicity grades are based on the NCI CTCAE Version 3.0., Allergy/Immunologic toxicity, GI toxicity, Renal toxicity, Hemorrhagic toxicity, Cardiovascular toxicity, Neurologic toxicity, Coagulation toxicity, Vascular toxicity, Pulmonary toxicity, Hepatic toxicity, Did the patient develop any of the following clinical sugns/symptoms of abnormal liver function during this assessment period, Indicated the etiology of the abnormal liver function, VOD, GVHD, Infection, Other, Unknown