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- Clinical Trial (206)
- Leukemia (114)
- Eligibility Determination (85)
- Hematology (37)
- Treatment Form (29)
- Leukemia, Myeloid, Acute (25)
- Laboratories (24)
- Myelodysplastic Syndromes (21)
- Follow-Up Studies (16)
- Routine documentation (14)
- Topotecan (13)
- Physical Examination (12)
- ALL (11)
- EHR (10)
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- Bone Marrow (6)
- Baseline (6)
- On-Study Form (6)
- Stem Cell Transplantation (5)
- Hematopoietic Stem Cell Transplantation (4)
- Concomitant Medication (4)
- Drug Therapy (4)
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- Multicenter Study (3)
- CML (3)
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269 Resultados de la búsqueda.
Itemgroups: Header, Patient demographics, Treatment Phase Information, Vital Status, Disease Follow-Up Status, Notice of Progression, RECOVERY, Transplant Treatment Plan, Notice of New Primary Cancer, Footer Module
Itemgroups: Header module, Laboratory assessments, CBC, Hematocrit, Hemoglobin, WBC, Neutrophils, Lymphocytes, Chemistry and LFT's, Creatinine, Bilirubin, AST, ALT
Itemgroups: ECOG clinical trial administrative data, Vital Status, Treatment Cycle Information, Comments, CCRR MODULE
Itemgroups: ECOG clinical trial administrative data, Adverse event assessment, Comments, CCRR MODULE
Itemgroups: ECOG clinical trial administrative data, Vital Status, High Dose Cytarabine Consolidation Therapy, Peripheral Bood Stem Cell Harvest, Gemtuzumab-ozogamicin Consolidation Therapy, Transplant Conditioning Regimen, PBSC Reinfusion, Transfusions, Comments, CCRR MODULE
Itemgroups: ECOG clinical trial administrative data, Non-protocol therapy, Comments, CCRR MODULE
Itemgroups: ECOG clinical trial administrative data, Diagnosis Second Primary Cancer, Comments, CCRR MODULE
Itemgroups: Header Module, Record the highest level of organ abnormalities, the etiologies contributing to the abnormalities and any biopsy results pertaining to GVHD during the assessment period, Skin etiologies, Upper intestinal tract etiologies, Lower intestinal tract etiologies, Liver etiologies
Itemgroups: Header Module, Record secondary discharge diagnoses
Itemgroups: Patient death, Enter appropriate cause of death code below. List in order of decreasing severity
Itemgroups: Patient infection medical history, Infection I, Infection II, Infection III, Provide agent(s) administered for this infectious period
Itemgroups: Header Module, Record date each apheresis was performed, For each selection procedure performed, record the following information, Starting HPC-A product #1, Starting HPC-A product #2, Starting HPC-A product #3, For each column used, record the following information, Pre-selection/post platelet & antibody wash product #1, Pre-selection/post platelet & antibody wash product #2, Pre-selection/post platelet & antibody wash product #3