Informações:
Falhas:
ID
20490
Descrição
SCRIPPS V: Intracoronary Brachytherapy for Recurrent Restenosis After Multiple Drug-Eluting Stents; ODM derived from: https://clinicaltrials.gov/show/NCT00714545
Link
https://clinicaltrials.gov/show/NCT00714545
Palavras-chave
Versões (1)
- 25/02/2017 25/02/2017 -
Transferido a
25 de fevereiro de 2017
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 NCT00714545
Eligibility Coronary Artery Disease NCT00714545
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT00714545
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Age
Item
1. age 18 years or older.
boolean
C0001779 (UMLS CUI [1])
Percutaneous coronary intervention
Item
2. eligible for percutaneous coronary intervention.
boolean
C1532338 (UMLS CUI [1])
Recurrent restenosis previously treated with des stents
Item
3. target lesion with recurrent restenosis (>50% by visual estimate) previously treated with any 2 or more combination of des stents.
boolean
C0333186 (UMLS CUI [1,1])
C1961379 (UMLS CUI [1,2])
C1961379 (UMLS CUI [1,2])
Angiography
Item
4. signs or symptoms of ischemia attributable to the target lesion, or stenosis > 50% by visual estimation of the lesion during angiography.
boolean
C0002978 (UMLS CUI [1])
Target lesion location
Item
5. target lesion is located within a native coronary artery or bypass graft.
boolean
C2986546 (UMLS CUI [1])
Protocol compliance
Item
6. be reliable, cooperative and willing to comply with all protocol-specified procedures and follow-up.
boolean
C0525058 (UMLS CUI [1])
Informed consent
Item
7. able to understand and sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Pregnancy
Item
1. confirmed pregnancy at the time of index pci.
boolean
C0032961 (UMLS CUI [1])
Hypersensitivity to aspirin, clopidogrel, ticlopidine
Item
2. has known allergies to aspirin, and to both clopidogrel (plavix ®) and ticlopidine (ticlid ®).
boolean
C0020517 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0040207 (UMLS CUI [3,2])
C0004057 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0040207 (UMLS CUI [3,2])
Contraindication to heparin and bivalirudin
Item
3. has known allergies or contraindication to heparin and bivalirudin (angiomax ®).
boolean
C1301624 (UMLS CUI [1,1])
C0019134 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0168273 (UMLS CUI [2,2])
C0019134 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0168273 (UMLS CUI [2,2])
Comorbidity
Item
4. has a significant medical condition which in the investigator's opinion may interfere with the patient's optimal participation in the study.
boolean
C0009488 (UMLS CUI [1])
Life expectancy
Item
5. any serious disease condition with life expectancy of less than 1 year.
boolean
C0023671 (UMLS CUI [1])
Coronary revascularization
Item
6. unsuccessful coronary revascularization procedure (residual stenosis > 30%).
boolean
C0877341 (UMLS CUI [1])
Angiographic evidence of thrombus
Item
7. angiographic evidence of thrombus.
boolean
C0087086 (UMLS CUI [1,1])
C0002971 (UMLS CUI [1,2])
C0002971 (UMLS CUI [1,2])
Intracoronary radiation
Item
8. no previous intracoronary radiation to the target artery.
boolean
C1522318 (UMLS CUI [1,1])
C0851346 (UMLS CUI [1,2])
C0851346 (UMLS CUI [1,2])