ID

16516

Description

A Study of Aspirin and Clopidogrel in Patients With Idiopathic Pulmonary Arterial Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00105209

Link

https://clinicaltrials.gov/show/NCT00105209

Keywords

  1. 7/21/16 7/21/16 -
Uploaded on

July 21, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Hypertension, Pulmonary NCT00105209

Eligibility Hypertension, Pulmonary NCT00105209

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of ipah
Description

diagnosis of ipah

Data type

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0152171
≥ 18 years of age
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
nyha functional class i, ii, or iii
Description

NYHA class

Data type

boolean

Alias
UMLS CUI [1]
C1275491
clinical stability (i.e., without change in pulmonary arterial hypertension medical regimen within one month prior to enrollment).
Description

clinical stability

Data type

boolean

Alias
UMLS CUI [1,1]
C0205360
UMLS CUI [1,2]
C0205210
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
other forms of pah
Description

other forms of pah

Data type

boolean

Alias
UMLS CUI [1,1]
C0020542
UMLS CUI [1,2]
C0015127
a contraindication to asa or clopidogrel
Description

a contraindication to asa or clopidogrel

Data type

boolean

Alias
UMLS CUI [1,1]
C3845816
UMLS CUI [1,2]
C0004057
UMLS CUI [2]
C1319916
thrombocytopenia (defined as platelet count ≤ 75,000)
Description

thrombocytopenia

Data type

boolean

Alias
UMLS CUI [1]
C0040034
history of intracranial hemorrhage or chronic thromboembolic disease
Description

history of intracranial hemorrhage or chronic thromboembolic disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0151699
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C2363973
renal failure
Description

renal failure

Data type

boolean

Alias
UMLS CUI [1]
C1533077
inability or unwillingness to avoid non-steroidal anti-inflammatory agents, asa, or warfarin use for the duration of the trial
Description

study compliance regarding NSAR, asa or warfarin refusal

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0003211
UMLS CUI [1,4]
C0004057
UMLS CUI [1,5]
C0043031

Similar models

Eligibility Hypertension, Pulmonary NCT00105209

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
diagnosis of ipah
Item
diagnosis of ipah
boolean
C0011900 (UMLS CUI [1,1])
C0152171 (UMLS CUI [1,2])
age
Item
≥ 18 years of age
boolean
C0001779 (UMLS CUI [1])
NYHA class
Item
nyha functional class i, ii, or iii
boolean
C1275491 (UMLS CUI [1])
clinical stability
Item
clinical stability (i.e., without change in pulmonary arterial hypertension medical regimen within one month prior to enrollment).
boolean
C0205360 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
other forms of pah
Item
other forms of pah
boolean
C0020542 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
a contraindication to asa or clopidogrel
Item
a contraindication to asa or clopidogrel
boolean
C3845816 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1319916 (UMLS CUI [2])
thrombocytopenia
Item
thrombocytopenia (defined as platelet count ≤ 75,000)
boolean
C0040034 (UMLS CUI [1])
history of intracranial hemorrhage or chronic thromboembolic disease
Item
history of intracranial hemorrhage or chronic thromboembolic disease
boolean
C0262926 (UMLS CUI [1,1])
C0151699 (UMLS CUI [1,2])
C0262926 (UMLS CUI [2,1])
C2363973 (UMLS CUI [2,2])
renal failure
Item
renal failure
boolean
C1533077 (UMLS CUI [1])
study compliance regarding NSAR, asa or warfarin refusal
Item
inability or unwillingness to avoid non-steroidal anti-inflammatory agents, asa, or warfarin use for the duration of the trial
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0003211 (UMLS CUI [1,3])
C0004057 (UMLS CUI [1,4])
C0043031 (UMLS CUI [1,5])

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