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Keywords
Lung Neoplasms ×
- Clinical Trial (298)
- Eligibility Determination (59)
- Treatment Form (45)
- Follow-Up Studies (45)
- Pulmonary Medicine (35)
- Registration (22)
- On-Study Form (22)
- Quality of Life (19)
- Adenocarcinoma (14)
- Laboratories (14)
- Baseline (12)
- Medical Oncology (12)
- Neoplasms (12)
- Topotecan (11)
- Adverse event (11)
- Pathology (10)
- Disease Response (9)
- Outcome Assessment (Health Care) (8)
- Carcinoma, Non-Small-Cell Lung (8)
- Small Cell Lung Carcinoma (8)
- Off-Treatment (8)
- Scores & Instruments (7)
- Released Standard (7)
- Non Small Cell Lung Cancer (6)
- Radiotherapy (5)
- Concomitant Medication (4)
- Clinical Protocols (4)
- Toxicity Tests (3)
- Breast Neoplasms (3)
- Trial screening (3)
- Neoplasm Metastasis (3)
- Prostatic Neoplasms (2)
- Radiology (2)
- Smoking (2)
- Urinalysis (2)
- Endometrial Neoplasms (2)
- Neoplasms, Squamous Cell (2)
- Body Surface Area (2)
- Body Weight (2)
- Chemistry, Clinical (2)
- Vital Signs (2)
- Pre-Study Form (2)
- Surgical Reporting Form (2)
- Document Tracking (2)
- Colonic Neoplasms (2)
- Demography (2)
- Electrocardiography (2)
- Hematology (2)
- Melanoma (2)
- Ovarian Neoplasms (2)
- Peritoneal Neoplasms (1)
- Appendix (1)
- Pharmacokinetics (1)
- Pheochromocytoma (1)
- Physical Examination (1)
- Adenomatous Polyposis Coli (1)
- Skin Neoplasms (1)
- Surgical Procedures, Operative (1)
- Survival (1)
- Testicular Neoplasms (1)
- Therapeutics (1)
- Thymus Neoplasms (1)
- Thyroid Neoplasms (1)
- Vulvar Neoplasms (1)
- Colorectal Neoplasms (1)
- Lymphoma, Large B-Cell, Diffuse (1)
- Smoking Cessation (1)
- Bupropion (1)
- Bile Duct Neoplasms (1)
- Biopsy (1)
- Clinical Trial, Phase II (1)
- Clinical Trial, Phase III (1)
- Urinary Bladder Neoplasms (1)
- Adrenocortical Carcinoma (1)
- Hemangioblastoma (1)
- Neuroendocrine Tumors (1)
- Brain Neoplasms (1)
- Clinical Chemistry Tests (1)
- Carcinoma (1)
- Carcinoma, Renal Cell (1)
- Carcinoma, Squamous Cell (1)
- Consolidation Chemotherapy (1)
- Epidemiological Monitoring (1)
- Symptom Assessment (1)
- Patient Outcome Assessment (1)
- Patient Reported Outcome (PRO) (1)
- Common Data Elements (CDE) (1)
- Patient information (1)
- Disease Status (1)
- Electrocardiogram (ECG) (1)
- Routine documentation (1)
- Cisplatin (1)
- Colonic Polyps (1)
- Death (1)
- Decision Making (1)
- Disease (1)
- Drug Therapy (1)
- Esophageal Neoplasms (1)
- Etoposide (1)
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329 Search results.
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: General information, Reporting Period, Footer Module
Itemgroups: Enrollment Requirements, Histologic Type, Histologic Grade, Pathological Attributes, Surgical-Pathological Results, Tissue Evaluation
Itemgroups: Header, Patient demographics, Data amendment, ON TREATMENT, OFF TREATMENT, Adverse Event Current Assessment, I. Non-Hematologic, II. GI Fistula , III. GI Perforations, IV. Pulmonary Hemorrhages, V. Non-Hematologic, VI. Infections, VII. Other Adverse Events, Footer Module
Itemgroups: RTOG clinical trial administrative data, REPORT ALL CONTINUING OR NEW ADVERSE EVENTS, Laboratory Procedure Date, Blood, Chemistries, Other studies
Itemgroups: Header, Patient demographics, Adverse event report, EXPECTED ADVERSE EVENTS
Itemgroups: Header Module, Patient demographics, Adverse Event Expedited Reporting System filed?, EXPECTED ADVERSE EVENTS
Itemgroups: Header Module, Patient demographics, Adverse Drug Reaction Report, Expected Adverse Events, Specify any other events that occurred during this time period., Footer Module
Itemgroups: Header, Patient demographics, Adverse event report, EXPECTED ADVERSE EVENTS
Itemgroups: 1. PATIENT INFORMATION, 2. MONTH OF REPORT, 3. PHYSICAL EXAM, 4. DISEASE STATUS, 5. SYSTEMIC THERAPY REPORT, NCIC CTG use only, Header, 6. NOTICE OF NEW PRIMARY, NCIC CTG use, 7. HEMATOLOGY, 8. BIOCHEMISTRY, 9. TREATMENT GIVEN SINCE LAST REPORT TO NCIC CTG, NCIC CTG use2, 10. ON TREATMENT LONG TERM TOXICITY, 11. COMMENTS, 12. HAVE YOU ATTACHED COPIES OF, 13. INVESTIGATOR SIGNATURE, CCRR MODULE
Itemgroups: 1. PATIENT INFORMATION, 2. CAUSE OF DEATH, 3. AUTOPSY, 4. OTHER MALIGNANCIES OR MARROW DYSPLASIA, NCIC CTG use, NCIC CTG use only, 5. TREATMENT GIVEN SINCE LAST REPORT TO NCIC CTG, NCIC CTG use2, 6. DELAYED TOXICITY/ADVERSE EVENT/INTERCURRENT ILLNESS, 7. COMMENTS, 8. HAVE YOU ATTACHED COPIES OF, 9. INVESTIGATOR SIGNATURE, CCRR MODULE
Itemgroups: SWOG clinical trial administrative data, Date of death, CAUSES OF DEATH, Comments