Information:
Fel:
ID
12968
Beskrivning
The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Patients With Ischemic Heart Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00121550
Länk
https://clinicaltrials.gov/show/NCT00121550
Nyckelord
Versioner (1)
- 2016-01-08 2016-01-08 -
Rättsinnehavare
CC BY-NC 3.0
Uppladdad den
8 januari 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Heart Disease NCT00121550
Eligibility Heart Disease NCT00121550
- StudyEvent: Eligibility
Similar models
Eligibility Heart Disease NCT00121550
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
age
Item
patients aged 18 to 85 years and
boolean
C0001779 (UMLS CUI [1])
myocardial infarction
Item
previous acute myocardial infarction (ami) or
boolean
C0027051 (UMLS CUI [1])
angina pectoris
Item
previous or present angina pectoris and
boolean
C0002962 (UMLS CUI [1])
informed concent
Item
signed informed concent
boolean
C0021430 (UMLS CUI [1])
ami or unstable angina pectoris within the last three months
Item
ami or unstable angina pectoris within the last three months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0002965 (UMLS CUI [2])
revascularisation
Item
revascularisation (ptca or cabg) within the preceding six months
boolean
C2936173 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C0010055 (UMLS CUI [2])
heart failure
Item
severe heart failure (new york heart association (nyha) functional class iv)
boolean
C1275491 (UMLS CUI [1])
known impaired renal or hepatic function
Item
known impaired renal or hepatic function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232741 (UMLS CUI [2])
malignancy
Item
active malignancy
boolean
C0006826 (UMLS CUI [1])
intolerance to macrolides
Item
intolerance to macrolides
boolean
C0020517 (UMLS CUI [1,1])
C0003240 (UMLS CUI [1,2])
C0003240 (UMLS CUI [1,2])
treatment with methylxanthines, carbamazepine, cisapride, astemizole, terfenadine, or coumarin anticoagulants
Item
treatment with methylxanthines, carbamazepine, cisapride, astemizole, terfenadine, or coumarin anticoagulants
boolean
C0066447 (UMLS CUI [1])
C0006949 (UMLS CUI [2])
C0072916 (UMLS CUI [3])
C0085170 (UMLS CUI [4])
C0085173 (UMLS CUI [5])
C0010206 (UMLS CUI [6])
C0006949 (UMLS CUI [2])
C0072916 (UMLS CUI [3])
C0085170 (UMLS CUI [4])
C0085173 (UMLS CUI [5])
C0010206 (UMLS CUI [6])
earlier inclusion in the claricor trial or participation in another drug trial within four weeks
Item
earlier inclusion in the claricor trial or participation in another drug trial within four weeks
boolean
C2348568 (UMLS CUI [1])
participation in other clinical trials within one month before this trial
Item
participation in other clinical trials within one month before this trial
boolean
C2348568 (UMLS CUI [1])
individuals incapable of managing own affairs or not able to sign written consent
Item
individuals incapable of managing own affairs or not able to sign written consent
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
lack of written consent
Item
lack of written consent
boolean
C0021430 (UMLS CUI [1])
women of childbearing age not using reliable contraceptives
Item
women of childbearing age not using reliable contraceptives
boolean
C0009871 (UMLS CUI [1])
breast feeding women
Item
breast feeding women
boolean
C0006147 (UMLS CUI [1])