CTC-AE+ Brazil 16 +17
Arpacore B.V.
Desenvolvido para iPad
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- R$ 14,90
- Oferece compras dentro do app
Capturas de tela
Descrição
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 CTC-AE 4 and CTC-AE 5 have been developed from the earlier vocabulary known as CTC (Common Toxicity Criteria). Each AE term is defined and accompanied by a grading scale that indicates the severity of the adverse event. All AE terms are organized by the System Organ Classes (SOCs) defined by the Medical Dictionary for Regulatory Activities (MedDRA).
Adverse events are common phenomena affecting patients being treated for cancer. With the availability of new agents and the multimodality interventions, it is critical to monitor systematically the AEs that are linked to oncology research.
CTCAE is fundamentally intended to be an agreed upon terminology for the designation, reporting, and grading of AEs that occur in oncology research.
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CTC-AE serves several purposes
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- To standardize AE reporting within the NCI oncology research community, across groups and modalities.
- To facilitate the evaluation of new cancer therapies, treatment modalities, and supportive measures.
- To aid in AE recognition and severity grading.
- To monitor safety data and for regulatory reporting.
- To define oncology research protocol parameters (e.g., eligibility criteria; dose-limiting toxicity; maximum tolerated dose; dose modification).
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KARNOFSKY and ECOG
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Additionally, CTC-AE+ now includes the two most common performance scores. As a reference and as a guided algorithm when necessary to add the event to the patient's record.
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ADVERSE EVENT LOGGER
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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. 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.
For convenience, all data can be exported as an excel CSV file to be imported into other analysis software.
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IMPORTANT NOTE
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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.
Novidades
Versão 3.1
Added CTC-4 and CTC-5 bookmarks for the most common adverse events.
Privacidade do app
Arpacore B.V., responsável pelo desenvolvimento do app, indicou que as práticas de privacidade do app podem incluir o gerenciamento de dados conforme descrito abaixo. Para mais informações, consulte sua política de privacidade.
Dados não coletados
Os desenvolvedores não coletam nenhum dado deste app.
As práticas de privacidade podem variar, por exemplo, com base nos recursos que você usa ou na sua idade. Saiba mais
Informações
- Venda
- Arpacore B.V.
- Tamanho
- 14,9 MB
- Categoria
- Medicina
- Compatibilidade
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- iPhone
- Requer o iOS 11.2 ou posterior.
- iPad
- Requer o iPadOS 11.2 ou posterior.
- iPod touch
- Requer o iOS 11.2 ou posterior.
- Mac
- Requer o macOS 11.0 ou posterior e um Mac com o chip M1 da Apple ou posterior.
- Apple Vision
- Requer o visionOS 1.0 ou posterior.
- Idiomas
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Inglês
- Classificação indicativa
- +17 Informação médica/tratamento frequente/intensa
- Copyright
- © Arpacore B.V.
- Preço
- R$ 14,90
- Compras dentro do app
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- Adverse Event Logger R$ 19,90