Informatie:
Fout:
Trefwoorden
Thérapie médicamenteuse adjuvante ×
- Clinical Trial (26)
- Drug trial (22)
- Clinical Trial, Phase II (16)
- Physical Examination (14)
- Blood (14)
- Laboratories (14)
- Stomach Neoplasms (8)
- Clinical Trial, Phase III (8)
- Clinical Laboratory Techniques (8)
- Ovarian Neoplasms (8)
- Medical Oncology (7)
- Clinical Trial, Phase I (6)
- Uterine Cervical Neoplasms (6)
- Cisplatin (6)
- Electrocardiogram (ECG) (5)
- Concomitant Medication (3)
- Molecular Biology (3)
- Biochemistry (2)
- Breast Neoplasms (2)
- Cytogenetics (2)
- Echocardiography (2)
- Gynecology (2)
- Office Visits (2)
- Peritoneal Neoplasms (1)
- Postoperative Complications (1)
- Pregnancy Tests (1)
- Radiology (1)
- Radiotherapy (1)
- Registries (1)
- Signs and Symptoms (1)
- General Surgery (1)
- Therapeutics (1)
- In Situ Hybridization, Fluorescence (1)
- Radiotherapy, Adjuvant (1)
- Hormone Replacement Therapy (1)
- Tobacco Use (1)
- Baseline (1)
- Treatment Form (1)
- General report (1)
- Non Small Cell Lung Cancer (1)
- Diphosphonates (1)
- Eligibility Determination (1)
- Fallopian Tube Neoplasms (1)
- Hematology (1)
- Medical History Taking (1)
Inhoudsopgave
Geselecteerde datamodellen
U moet ingelogd zijn om meerdere datamodellen te selecteren en die te downloaden of te analyseren.
41 Zoekresultaten.
Itemgroepen: Chemotherapy, Therapeutic regimen, ADJUVANT THERAPY
Itemgroepen: National Quality Register for Breast Cancer, Pre- or post operative adjuvant oncological treatment, Chemotherapy, Radiotherapy, Endocrine treatment, Antibody therapy, Bisphosphonates therapy
Itemgroepen: Administrative, Prior Ovarian Cancer Treatment - Chemotherapy, Has the patient received radiotherapy?, Prior Ovarian Cancer Treatment - Radiotherapy , Has the patient received prior cancer-related surgery?, Prior Ovarian Cancer Treatment - Surgical Treatment , Has the patient received other cancer-related treatments?, Other Cancer Related Treatments, Laboratory Tests (within 7 days prior to Day 1) - Haematology, Laboratory Tests (within 7 days prior to Day 1) - Haematology , Laboratory Tests (within 7 days prior to Day 1) - Chemistry, Laboratory Tests (within 7 days prior to Day 1) - Chemistry , Lesion Assessment Record
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Diagnostic procedures, Results, Progress, Administrative Documentation
Itemgroepen: Administrative Documentation, Adverse Event, Physical Examination, Laboratory Data, Disease Progression, Diagnostic procedures, Postoperative Chemotherapy, Capecitabine, Life quality, Administrative Documentation
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Disease Progression, Additive Chemotherapy, Capecitabine, Life quality, Adverse Event, Administrative Documentation
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Additive Chemotherapy, Capecitabine, Adverse Event, Administrative Documentation
Itemgroepen: Administrative Documentation, Hospital stay information, Physical Examination, Laboratory Data, Non-surgical Complications, Surgical Complications, Adverse Event, Administrative Documentation
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Diagnostic procedures, Results, Disease Progression, Adverse Event, Administrative Documentation
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Disease Progression, Preoperative Chemotherapy, Capecitabine, Adverse Event, Administrative Documentation
Itemgroepen: Administrative Documentation, Physical Examination, Laboratory Data, Disease Progression, Preoperative Chemotherapy, Capecitabine, Adverse Event, Administrative Documentation
Itemgroepen: Visit 12: Fourth cycle of post-OP Chemotherapy, Status of Patient and recording of CTCAE, Postoperative intravenous chemotherapy, Course of chemotherapy cycle, Confirmation of correctness