ID

34544

Beschrijving

3D Echo Evaluation of the Ventricles in Sclero Associated Severe PAH; ODM derived from: https://clinicaltrials.gov/show/NCT02207868

Link

https://clinicaltrials.gov/show/NCT02207868

Trefwoorden

  1. 19-01-19 19-01-19 -
  2. 22-05-19 22-05-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Pulmonary Arterial Hypertension NCT02207868

Eligibility Pulmonary Arterial Hypertension NCT02207868

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age >17
Beschrijving

ID.1

Datatype

boolean

pulmonary arterial hypertension (pah) associated with who group 1 who start a parenteral prostanoid-therapy
Beschrijving

ID.2

Datatype

boolean

written informed consent
Beschrijving

ID.3

Datatype

boolean

prostanoid naive
Beschrijving

ID.4

Datatype

boolean

no change of the pah specific therapy within 3 weeks of the recruitment to the study
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy and lactation period
Beschrijving

ID.6

Datatype

boolean

women of child bearing potential who do not use an effective and secure method for birth control
Beschrijving

ID.7

Datatype

boolean

severe chronic kidney insufficiency (glomerular filtration rate <30), which will remain for more than 3 months
Beschrijving

ID.8

Datatype

boolean

liver-insufficiency child c
Beschrijving

ID.9

Datatype

boolean

life expectancy shorter than the course of the study (for example because of malignant disease
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Pulmonary Arterial Hypertension NCT02207868

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age >17
boolean
ID.2
Item
pulmonary arterial hypertension (pah) associated with who group 1 who start a parenteral prostanoid-therapy
boolean
ID.3
Item
written informed consent
boolean
ID.4
Item
prostanoid naive
boolean
ID.5
Item
no change of the pah specific therapy within 3 weeks of the recruitment to the study
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
pregnancy and lactation period
boolean
ID.7
Item
women of child bearing potential who do not use an effective and secure method for birth control
boolean
ID.8
Item
severe chronic kidney insufficiency (glomerular filtration rate <30), which will remain for more than 3 months
boolean
ID.9
Item
liver-insufficiency child c
boolean
ID.10
Item
life expectancy shorter than the course of the study (for example because of malignant disease
boolean

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