ID

33926

Beschrijving

A Comparison Between Paclitaxel-eluting Balloon in Combination With BMS Implantation vs Conventional Balloon and DES Implantation; ODM derived from: https://clinicaltrials.gov/show/NCT01637896

Link

https://clinicaltrials.gov/show/NCT01637896

Trefwoorden

  1. 08-01-19 08-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

8 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Myocardial Ischemia NCT01637896

Eligibility Myocardial Ischemia NCT01637896

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age> 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
angina or stress test positive for ischemia
Beschrijving

Angina Pectoris | Stress Test Positive Ischemia

Datatype

boolean

Alias
UMLS CUI [1]
C0002962
UMLS CUI [2,1]
C3494508
UMLS CUI [2,2]
C1514241
UMLS CUI [2,3]
C0022116
de novo coronary stenosis>50%
Beschrijving

Coronary Stenosis de novo Percentage

Datatype

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C1515568
UMLS CUI [1,3]
C0439165
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
recent myocardial infarction (<72h)
Beschrijving

Recent myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1998297
severe chronic kidney disease
Beschrijving

Chronic Kidney Disease Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0205082
allergy to paclitaxel
Beschrijving

Paclitaxel allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0570707
contraindication for combined antiplatelet treatment
Beschrijving

Medical contraindication Antiplatelet therapy Combined

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1096021
UMLS CUI [1,3]
C0205195
life expectancy <1 year
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
hypersensitivity or contraindication to one of the study drugs
Beschrijving

Hypersensitivity Investigational New Drugs | Medical contraindication Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0013230
lack of consent
Beschrijving

Informed Consent Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268

Similar models

Eligibility Myocardial Ischemia NCT01637896

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age> 18 years
boolean
C0001779 (UMLS CUI [1])
Angina Pectoris | Stress Test Positive Ischemia
Item
angina or stress test positive for ischemia
boolean
C0002962 (UMLS CUI [1])
C3494508 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
C0022116 (UMLS CUI [2,3])
Coronary Stenosis de novo Percentage
Item
de novo coronary stenosis>50%
boolean
C0242231 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Recent myocardial infarction
Item
recent myocardial infarction (<72h)
boolean
C1998297 (UMLS CUI [1])
Chronic Kidney Disease Severe
Item
severe chronic kidney disease
boolean
C1561643 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Paclitaxel allergy
Item
allergy to paclitaxel
boolean
C0570707 (UMLS CUI [1])
Medical contraindication Antiplatelet therapy Combined
Item
contraindication for combined antiplatelet treatment
boolean
C1301624 (UMLS CUI [1,1])
C1096021 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
Life Expectancy
Item
life expectancy <1 year
boolean
C0023671 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Medical contraindication Investigational New Drugs
Item
hypersensitivity or contraindication to one of the study drugs
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Informed Consent Lacking
Item
lack of consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])

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