ID

28506

Beschreibung

Zotarolimus and Everolimus-Eluting Stents ProsPectively Compared in Real World; ODM derived from: https://clinicaltrials.gov/show/NCT00768846

Link

https://clinicaltrials.gov/show/NCT00768846

Stichworte

Versionen (1)
  1. 20.01.18 20.01.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

20. Januar 2018

DOI

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Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00768846

Englisch

Eligibility Coronary Artery Disease NCT00768846

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients older than 18 years with symptomatic coronary artery disease undergoing pci with stent implantation.
Beschreibung

Age | Coronary Artery Disease Symptomatic | Percutaneous Coronary Intervention | Placement of stent

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C1956346
UMLS CUI [2,2]
C0231220
UMLS CUI [3]
C1532338
UMLS CUI [4]
C0522776
written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
Beschreibung

Informed Consent | Informed Consent Patient Representative

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0030701
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiogenic shock.
Beschreibung

Shock, Cardiogenic

Datentyp

boolean

Alias
UMLS CUI [1]
C0036980
malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
Beschreibung

Malignant Neoplasms Protocol Compliance Lacking | Comorbidity Protocol Compliance Lacking | Life Expectancy | Liver disease Severe | Kidney Disease Severe | Pancreatic Disease Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0525058
UMLS CUI [1,3]
C0332268
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0525058
UMLS CUI [2,3]
C0332268
UMLS CUI [3]
C0023671
UMLS CUI [4,1]
C0023895
UMLS CUI [4,2]
C0205082
UMLS CUI [5,1]
C0022658
UMLS CUI [5,2]
C0205082
UMLS CUI [6,1]
C0030286
UMLS CUI [6,2]
C0205082
known allergy to the study medications: everolimus, zotarolimus, cobalt chrome.
Beschreibung

Hypersensitivity Investigational New Drugs | Hypersensitivity Everolimus | Hypersensitivity Zotarolimus | Hypersensitivity Cobalt Chrome

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0541315
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C1700035
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0008576
inability to take clopidogrel for at least 6 months.
Beschreibung

Clopidogrel Intake Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0070166
UMLS CUI [1,2]
C1512806
UMLS CUI [1,3]
C1299582
pregnancy (present, suspected or planned) or positive pregnancy test. (in women with childbearing potential a pregnancy test is mandatory.)
Beschreibung

Pregnancy | Pregnancy Suspected | Pregnancy, Planned | Pregnancy test positive | Childbearing Potential Requirement Pregnancy Test

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0750491
UMLS CUI [3]
C0032992
UMLS CUI [4]
C0240802
UMLS CUI [5,1]
C3831118
UMLS CUI [5,2]
C1514873
UMLS CUI [5,3]
C0032976
previous enrollment in this trial.
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
patient's inability to fully cooperate with the study protocol.
Beschreibung

Protocol Compliance Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
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Ähnliche Modelle

Eligibility Coronary Artery Disease NCT00768846

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age | Coronary Artery Disease Symptomatic | Percutaneous Coronary Intervention | Placement of stent
Item
patients older than 18 years with symptomatic coronary artery disease undergoing pci with stent implantation.
boolean
C0001779 (UMLS CUI [1])
C1956346 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C1532338 (UMLS CUI [3])
C0522776 (UMLS CUI [4])
Informed Consent | Informed Consent Patient Representative
Item
written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Shock, Cardiogenic
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Malignant Neoplasms Protocol Compliance Lacking | Comorbidity Protocol Compliance Lacking | Life Expectancy | Liver disease Severe | Kidney Disease Severe | Pancreatic Disease Severe
Item
malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
boolean
C0006826 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C0023671 (UMLS CUI [3])
C0023895 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0022658 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0030286 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
Hypersensitivity Investigational New Drugs | Hypersensitivity Everolimus | Hypersensitivity Zotarolimus | Hypersensitivity Cobalt Chrome
Item
known allergy to the study medications: everolimus, zotarolimus, cobalt chrome.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0541315 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1700035 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0008576 (UMLS CUI [4,2])
Clopidogrel Intake Unable
Item
inability to take clopidogrel for at least 6 months.
boolean
C0070166 (UMLS CUI [1,1])
C1512806 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Pregnancy | Pregnancy Suspected | Pregnancy, Planned | Pregnancy test positive | Childbearing Potential Requirement Pregnancy Test
Item
pregnancy (present, suspected or planned) or positive pregnancy test. (in women with childbearing potential a pregnancy test is mandatory.)
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0032992 (UMLS CUI [3])
C0240802 (UMLS CUI [4])
C3831118 (UMLS CUI [5,1])
C1514873 (UMLS CUI [5,2])
C0032976 (UMLS CUI [5,3])
Study Subject Participation Status
Item
previous enrollment in this trial.
boolean
C2348568 (UMLS CUI [1])
Protocol Compliance Unable
Item
patient's inability to fully cooperate with the study protocol.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
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