ID

14211

Beschrijving

Anakinra to Prevent Adverse Post-infarction Remodeling (2); ODM derived from: https://clinicaltrials.gov/show/NCT01175018

Link

https://clinicaltrials.gov/show/NCT01175018

Trefwoorden

  1. 04-04-16 04-04-16 -
Geüploaded op

4 april 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Myocardial Infarction NCT01175018

Eligibility Acute Myocardial Infarction NCT01175018

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with stemi will be asked to enroll according to the following inclusion criteria:
Beschrijving

ST segment elevation myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1536220
age > 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
acute (<12 h) onset of chest pain associated with st segment elevation (>2 mm) in 2 or more anatomically contiguous leads at ecg,
Beschrijving

acute (<12 h) onset of chest pain

Datatype

boolean

Alias
UMLS CUI [1]
C2073320
successful primary percutaneous coronary intervention
Beschrijving

Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C1532338
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to give informed consent
Beschrijving

inability to give informed consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
unsuccessful revascularization procedure
Beschrijving

Myocardial Revascularization

Datatype

boolean

Alias
UMLS CUI [1]
C0027056
hemodynamic instability including hypotension
Beschrijving

Hemodynamic instability

Datatype

boolean

Alias
UMLS CUI [1]
C0948268
prior q-wave ami
Beschrijving

Pathological Q wave

Datatype

boolean

Alias
UMLS CUI [1]
C0429090
end-stage congestive heart failure (aha/acc class c-d, new york heart association iv), severe left ventricular dysfunction (ef<20%)
Beschrijving

Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
severe valvular heart disease
Beschrijving

Heart valve disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018824
pregnancy, dye allergy or contraindications to cardiac angiography and/or magnetic resonance imaging, coagulopathy (inr>1.5 or platelet count<50000/mm3),
Beschrijving

Pregnancy, Allergy to dye

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0694573
recent (<14 days) use of anti-inflammatory drugs (not including nsaids)
Beschrijving

Anti-Inflammatory Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0003209
chronic inflammatory disease (including but not limited to rheumatoid arthritis, systemic lupus erythematosus), and malignancy or any comorbidity limiting survival or conditions predicting inability to complete the study.
Beschrijving

Chronic inflammatory disorder

Datatype

boolean

Alias
UMLS CUI [1]
C1290886

Similar models

Eligibility Acute Myocardial Infarction NCT01175018

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ST segment elevation myocardial infarction
Item
patients with stemi will be asked to enroll according to the following inclusion criteria:
boolean
C1536220 (UMLS CUI [1])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
acute (<12 h) onset of chest pain
Item
acute (<12 h) onset of chest pain associated with st segment elevation (>2 mm) in 2 or more anatomically contiguous leads at ecg,
boolean
C2073320 (UMLS CUI [1])
Percutaneous Coronary Intervention
Item
successful primary percutaneous coronary intervention
boolean
C1532338 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
inability to give informed consent
Item
inability to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
Myocardial Revascularization
Item
unsuccessful revascularization procedure
boolean
C0027056 (UMLS CUI [1])
Hemodynamic instability
Item
hemodynamic instability including hypotension
boolean
C0948268 (UMLS CUI [1])
Pathological Q wave
Item
prior q-wave ami
boolean
C0429090 (UMLS CUI [1])
Congestive heart failure
Item
end-stage congestive heart failure (aha/acc class c-d, new york heart association iv), severe left ventricular dysfunction (ef<20%)
boolean
C0018802 (UMLS CUI [1])
Heart valve disease
Item
severe valvular heart disease
boolean
C0018824 (UMLS CUI [1])
Pregnancy, Allergy to dye
Item
pregnancy, dye allergy or contraindications to cardiac angiography and/or magnetic resonance imaging, coagulopathy (inr>1.5 or platelet count<50000/mm3),
boolean
C0032961 (UMLS CUI [1])
C0694573 (UMLS CUI [2])
Anti-Inflammatory Agents
Item
recent (<14 days) use of anti-inflammatory drugs (not including nsaids)
boolean
C0003209 (UMLS CUI [1])
Chronic inflammatory disorder
Item
chronic inflammatory disease (including but not limited to rheumatoid arthritis, systemic lupus erythematosus), and malignancy or any comorbidity limiting survival or conditions predicting inability to complete the study.
boolean
C1290886 (UMLS CUI [1])

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