Télécharger CTC-AE+ sur PC

                   


Sinon, suivez les instructions ci-dessous pour utiliser CTC-AE+ sur PC:

CTC-AE+ Sur iTunes

CTC-AE+ is a browsable reference to the CTC-AE list of adverse event (AE) terms commonly encountered in oncology, plus a portable Adverse Event Logger to keep track of all adverse events during a clinical study.  The Adverse Event Logger is a structured local database to help the investigator to keep track of all the adverse events related to the patients participating in a clinical trial.  It is possible to track multiple clinical studies, multiple patients per clinical trial and multiple events per patient.  Adverse events are common phenomena affecting patients being treated for cancer.  cette application is fundamentally intended to be an agreed upon terminology for the designation, reporting, and grading of AEs that occur in oncology research.  - To define oncology research protocol parameters (e.g., eligibility criteria; dose-limiting toxicity; maximum tolerated dose; dose modification).  This application is strictly EU GDPR compliant and no clinical study or patient information is saved outside the device or uploaded to any remote cloud resources.  Each AE term is defined and accompanied by a grading scale that indicates the severity of the adverse event.  Events can be selected from the CTC-AE 4 and CTC-AE 5 databases, from Karnofsky and ECOG score tables or can be entered as customized events.  With the availability of new agents and the multimodality interventions, it is critical to monitor systematically the AEs that are linked to oncology research.  - To standardize AE reporting within the NCI oncology research community, across groups and modalities.  All AE terms are organized by the System Organ Classes (SOCs) defined by the Medical Dictionary for Regulatory Activities (MedDRA).  As a reference and as a guided algorithm when necessary to add the event to the patient's record.  The CTC-AE 4 and CTC-AE 5 have been developed from the earlier vocabulary known as CTC (Common Toxicity Criteria).  - To facilitate the evaluation of new cancer therapies, treatment modalities, and supportive measures.  For convenience, all data can be exported as an excel CSV file to be imported into other analysis software.  - To monitor safety data and for regulatory reporting.  Additionally, CTC-AE+ now includes the two most common performance scores.