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- Clinical Trial (344)
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380 Resultados de la búsqueda.
Itemgroups: Patientendaten, Clinical finding, Differential blood count, Klinische Chemie, 5-Azacytidine, 5-Azacytidine - Dose no. 1, 5-Azacytidine - Dose no. 2, 5-Azacytidine - Dose no. 3, 5-Azacytidine - Dose no. 4, 5-Azacytidine - Dose no. 5, 5-Azacytidine dose reduction, Transfusions, Chemotherapy, Ara-C , Daunorubicin, G-CSF, Cytopenia duration, Leukopenia, Neutropenia, Thrombopenia, Unterschrift
Itemgroups: Header, ON TREATMENT, OFF TREATMENT, Section I, Section II, Response
Itemgroups: Header Module, Reporting Period, Header, Vital Status, Preparative Conditioning Regimen, Preparative Conditioning Regimen1, Donor Information, Allogeneic Transplant, Footer Module
Itemgroups: Eligibility, Demographics, Data correct
Itemgroups: Header, Completed by submitting institutions, Completed by central lab
Itemgroups: Header Module, Reporting Period, Header, Patient Information, Leukemia Classification/Baseline Evaluation Data, Pre-registration Disease Assessment, Prior Treatment, Pre-registration Hematology/Chemistry, Pre-registration Evaluation, Comorbidities, Pre-registration Evaluation1, HLA Typing, Baseline Abnormalities, Footer Module
Itemgroups: Allgemeine Angaben, Tägliche Aktivitäten, Gehen, Gelenkinspektion, Bewegungsumfang (in °) Hüftgelenk, Bewegungsumfang (in °) Kniegelenk, Bewegungsumfang (in °) Sprunggelenk, Muskelbefund Oberschenkel, Muskelbefund Unterschenkel, Therapiekomplikationen, Begleitmedikation, Spez. Intervention gegen Osteonekrosen, Bemerkungen
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
Itemgroups: Protocol Administration, Patient Demographics/Pre-Treatment Characteristics, Certification Of Eligibility, Protocol Design, Initial Patient Consent For Specimen Use, Registration Information, CCRR MODULE
Itemgroups: Patientendaten, 5-Azacytidine - Dose no. 1, 5-Azacytidine - Dose no. 2, 5-Azacytidine - Dose no. 3, 5-Azacytidine - Dose no. 4, 5-Azacytidine - Dose no. 5, 5-Azacytidine dose reduction, Differentialblutbild, Chemotherapy, Ara-C , Daunorubicin, G-CSF, Cytopenia duration, leukopenia, neutropenia, thrombopenia, Unterschrift
Itemgroups: Clinical finding, Differential blood count, Klinische Chemie, 5-Azacytidine, 5-Azacytidine - Dose, 5-Azacytidine dose reduction, Transfusions, Chemotherapy, Ara-C, G-CSF, Cytopenia duration, Leukopenia, Neutropenia, Thrombopenia, Signature
Itemgroup: Patient demographics