Informações:
Falhas:
ID
44467
Descrição
Atorvastatin Plus Ezetimibe on Coronary Plaque Progression; ODM derived from: https://clinicaltrials.gov/show/NCT01086020
Link
https://clinicaltrials.gov/show/NCT01086020
Palavras-chave
Versões (2)
- 14/12/2018 14/12/2018 -
- 27/09/2021 27/09/2021 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
27 de setembro de 2021
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Coronary Artery Disease NCT01086020
Eligibility Coronary Artery Disease NCT01086020
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT01086020
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Coronary angiography Willing | Percutaneous Coronary Intervention potential Willing
Item
willing to receive the coronary angiography and potential pci therapy
boolean
C0085532 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C3245505 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
C0600109 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C3245505 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Statins
Item
patients was treated by statins before randomization
boolean
C0360714 (UMLS CUI [1])
Coronary Stenosis Percentage | Target Lesion
Item
patient with ≤ 20% and ≥ 70% coronary narrowing and target lesion
boolean
C0242231 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C2986546 (UMLS CUI [2])
C0439165 (UMLS CUI [1,2])
C2986546 (UMLS CUI [2])
ST elevation myocardial infarction Duration
Item
st elevation myocardial infarction less than 7 days
boolean
C1536220 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Informed Consent Lacking
Item
without informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
abnormal liver function before randomization, (ast, alt ≥uln)
boolean
C0086565 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
Hepatitis | Myopathy
Item
active hepatitis or muscular disease
boolean
C0019158 (UMLS CUI [1])
C0026848 (UMLS CUI [2])
C0026848 (UMLS CUI [2])
Renal Insufficiency | Creatinine measurement, serum
Item
impaired renal function with serum creatinine level > 3mg/dl
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0201976 (UMLS CUI [2])
Impaired left ventricular function | Left ventricular ejection fraction
Item
impaired left ventricular function with lvef > 30%
boolean
C0242698 (UMLS CUI [1])
C0428772 (UMLS CUI [2])
C0428772 (UMLS CUI [2])
Study Subject Participation Status
Item
participate in other studies
boolean
C2348568 (UMLS CUI [1])