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Keywords
H01.158.273.343.750 ×
- Clinical Trial (4)
- Breast Neoplasms (3)
- Gynecology (3)
- Adverse event (2)
- Clinical Trial, Phase I (1)
- Clinical Trial, Phase III (1)
- Brain Neoplasms (1)
- Concomitant Medication (1)
- End of Study (1)
- Drug trial (1)
- Informed Consent (1)
- Neoplasm Metastasis (1)
- Ovarian Neoplasms (1)
Sommario
Modelli di dati selezionati
Devi effettuare il log in per selezionare i modelli di dati da scaricare per successive analisi
4 Risultati di ricerca.
Itemgroups: Date of visit, Pharmacogenetic Test, Informed Consent, Pharmacogenetic Test, Informed Consent, Withdraw
Itemgroups: Date of visit, Assessment Date, Event Log, Status, Non-serious Adverse Event, Serious Adverse Event, Concomitant Agent, Concomitant Agent, Adrenal Cortex Hormones, Blood product; Supportive care, Collection of blood specimen for laboratory procedure, Pharmacogenetic Test, Informed Consent, Pharmacogenetic Test, Informed Consent, Withdraw (activity)
Itemgroups: Administrative Data, PGx-Pharmacogenetic Research Consent, PGx-Pharmacogenetic Research Withdrawal of Consent
Itemgroups: Header, investigational product discontinuation, PGx-Pharmacogenetic Research, Concomitant Medications, If Yes to Concominant Medication, Non-serious adverse events, Non-serious adverse events, Serious adverse event, Serious adverse events description, Seriousness, Document section Demography data, SECTION 4, Section 5, Relevant Medical Conditions, Document section Risk factors, Document section Concomitant Medications, Drug Details, Assessments, Document section, Pregnancy information, Death, Study Conclusion, Investigator comment log, Investigators Signature