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Keywords
SKF104864A ×
- Clinical Trial (19)
- AML (13)
- Myelodysplastic Syndromes (13)
- Lung Neoplasms (11)
- Medical Oncology (10)
- Laboratories (8)
- Adverse event (7)
- Small Cell Lung Carcinoma (6)
- Clinical Trial, Phase III (5)
- Carcinoma (5)
- Cisplatin (5)
- Carcinoma, Non-Small-Cell Lung (4)
- Concomitant Medication (4)
- Trial screening (4)
- Hematology (3)
- Rectal Neoplasms (2)
- Urinalysis (2)
- Toxicity Tests (2)
- Body Surface Area (2)
- Body Weight (2)
- Chemistry, Clinical (2)
- Vital Signs (2)
- Drug trial (2)
- Electrocardiography (2)
- Ovarian Neoplasms (2)
- Physical Examination (1)
- Quality of Life (1)
- Radiotherapy (1)
- Sarcoma (1)
- Drugs, Investigational (1)
- Sex Cord-Gonadal Stromal Tumors (1)
- Blood Transfusion (1)
- Clinical Chemistry Tests (1)
- Lost to Follow-Up (1)
- Drug-Related Side Effects and Adverse Reactions (1)
- Specimen (1)
- Disease Response (1)
- End of Study (1)
- Electrocardiogram (ECG) (1)
- Non Small Cell Lung Cancer (1)
- Demography (1)
- Eligibility Determination (1)
- Etoposide (1)
- Follow-Up Studies (1)
- Giant Cell Tumors (1)
- Gynecology (1)
- Histology (1)
- Medical History Taking (1)
- Anti-Bacterial Agents (1)
- Neoplasms (1)
- Neoplasms by Site (1)
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Modelli di dati selezionati
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32 Risultati di ricerca.
Itemgroups: Identification Numbers, Laboratory Tests-Hematology, Laboratory Tests-Blood Chemistry, Laboratory Tests-Urinalysis, Laboratory Tests-Bone Marrow Examination, Cytogenetics
Itemgroups: Identification Numbers, Laboratory Tests-Hematology, Laboratory Tests-Blood Chemistry, Laboratory Tests-Urinalysis, Laboratory Tests-Bone Marrow Examination, Cytogenetics
Itemgroups: Administrative, Laboratory Reference Ranges, Laboratory Reference Ranges , Concomitant Medication - Continued, Adverse Experiences (Non-serious), Adverse Experiences (Non-serious), Investigator's Signature (Adverse Experience)
Itemgroups: Administrative, Serious Adverse Experiences, Vital Signs , 12-Lead Electrocardiogram
Itemgroups: Administrative, Laboratory Tests - Haematology, Laboratory Tests - Blood Chemistry, Laboratory Tests - Urinalysis
Itemgroups: Administrative, Course Delay (Regimen 1, Regimen 2), Weight/Body Surface Area (Regimen 1, Regimen 2), Topotecan Study Medication Record (Regimen 1, Regimen 2), Topotecan Study Medication Record (Regimen 1, Regimen 2), Day 5 Pre-Cisplatin Hydration Record (Regimen 1), Day 5 Cisplatin Study Medication Record (Regimen 1), Cisplatin Study Medication Record, Day 5 Post-Cisplatin Hydration Record (Regimen 1), Day 5 Vital Signs, Post-Cisplatin Dosing (Regimen 1), Etoposide Study Medication Record (Regimen 2), Etoposide Study Medication Record , Day 5 Vital Signs, Post-Etoposide Dosing (Regimen 2)
Itemgroups: Administrative, Weight/Body Surface Area (Regimen 1, Regimen 2), Topotecan Study Medication Record (Regimen 1, Regimen 2), Day 5 Pre-Cisplatin Hydration Record (Regimen 1), Day 5 Cisplatin Study Medication Record (Regimen 1), Day 5 Post-Cisplatin Hydration Record (Regimen 1), Day 5 Vital Signs, Post-Cisplatin Dosing (Regimen 1), Etoposide Study Medication Record (Regimen 1, Regimen 2), Day 5 Vital Signs, Post-Etoposide Dosing (Regimen 2)
Itemgroups: Administrative, Concomitant Medication, Adverse Experiences (Non-serious), Adverse Experiences (Non-serious), Investigator's Signature (Adverse Experience), Course Conclusion, Investigator's Signature (Study Conclusion)
Itemgroups: Administrative, Serious Adverse Experiences, Vital Signs , 12-Lead Electrocardiogram
Itemgroups: Administrative, Laboratory Tests - Haematology, Laboratory Tests - Blood Chemistry, Laboratory Tests - Urinalysis
Itemgroups: Administrative, Inclusion Criteria, Exclusion Criteria, Inclusion/ Exclusion, Investigator's Signature
Itemgroups: Administrative, Prior and Concomitant Medication, Prior and Concomitant Medication , Telephone Randomisation