ID

37087

Beschrijving

Red Yeast Rice and Subclinical Atherosclerosis in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT02257047

Link

https://clinicaltrials.gov/show/NCT02257047

Trefwoorden

Versies (1)
  1. 02-07-19 02-07-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 juli 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT02257047

Engels

Eligibility Rheumatoid Arthritis NCT02257047

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with a definite diagnose of rheumatoid arthritis(ra) were included if they met the classification criteria for ra established by the american rheumatism association (acr) and european league against rheumatism (eular) in 2010
Beschrijving

Rheumatoid Arthritis | Classification Criteria Fulfill

Datatype

boolean

Alias
UMLS CUI [1]
C0003873
UMLS CUI [2,1]
C0008902
UMLS CUI [2,2]
C0243161
UMLS CUI [2,3]
C1550543
aged from 18 to 75 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
without conflict to the written, informed consent signed prior to the enrollment
Beschrijving

Informed Consent | Conflict Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0009671
UMLS CUI [2,2]
C0332197
no severe hepatic or renal disorders
Beschrijving

Liver disease Severe Absent | Kidney Disease Severe Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C0022658
UMLS CUI [2,2]
C0205082
UMLS CUI [2,3]
C0332197
no known carotid artery stenosis
Beschrijving

Carotid Stenosis Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007282
UMLS CUI [1,2]
C0332197
no coagulation disorders
Beschrijving

Blood Coagulation Disorder Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0332197
no hypertension
Beschrijving

Hypertensive disease Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0332197
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
being in pregnancy, lactation period or under a pregnancy plan
Beschrijving

Pregnancy | Breast Feeding | Pregnancy, Planned

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
being allergic to the test drug
Beschrijving

Hypersensitivity Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
not compatible for the trial medication
Beschrijving

Incompatibility Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0679426
UMLS CUI [1,2]
C0013230
without full legal capacity
Beschrijving

Legal capacity Limited

Datatype

boolean

Alias
UMLS CUI [1,1]
C0683673
UMLS CUI [1,2]
C0439801
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Similar models

Eligibility Rheumatoid Arthritis NCT02257047

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Rheumatoid Arthritis | Classification Criteria Fulfill
Item
patients with a definite diagnose of rheumatoid arthritis(ra) were included if they met the classification criteria for ra established by the american rheumatism association (acr) and european league against rheumatism (eular) in 2010
boolean
C0003873 (UMLS CUI [1])
C0008902 (UMLS CUI [2,1])
C0243161 (UMLS CUI [2,2])
C1550543 (UMLS CUI [2,3])
Age
Item
aged from 18 to 75 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent | Conflict Absent
Item
without conflict to the written, informed consent signed prior to the enrollment
boolean
C0021430 (UMLS CUI [1])
C0009671 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Liver disease Severe Absent | Kidney Disease Severe Absent
Item
no severe hepatic or renal disorders
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Carotid Stenosis Absent
Item
no known carotid artery stenosis
boolean
C0007282 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Blood Coagulation Disorder Absent
Item
no coagulation disorders
boolean
C0005779 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Hypertensive disease Absent
Item
no hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
being in pregnancy, lactation period or under a pregnancy plan
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Hypersensitivity Investigational New Drugs
Item
being allergic to the test drug
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Incompatibility Investigational New Drugs
Item
not compatible for the trial medication
boolean
C0679426 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Legal capacity Limited
Item
without full legal capacity
boolean
C0683673 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
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