ID

36568

Descripción

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

Palabras clave

Versiones (2)
  1. 19/1/19 19/1/19 -
  2. 22/5/19 22/5/19 -
Titular de derechos de autor

Regina Steringer-Mascherbauer, Elisabethinen Hospital Linz

Subido en

22 de mayo de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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3D Echo Evaluation of Ventricles in Severe PAH NCT02207868

Inglés

Eligibility Criteria

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
age >17
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
pulmonary arterial hypertension (PAH) associated with WHO group 1 who start a parenteral prostanoid-therapy
Descripción

pulmonary arterial hypertension (WHO grouping) starting a parenteral prostanoid-therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2973725
UMLS CUI [1,2]
C4267671
UMLS CUI [2,1]
C1704686
UMLS CUI [2,2]
C0033554
UMLS CUI [2,3]
C0678823
written informed consent
Descripción

written informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
prostanoid naive
Descripción

prostanoid naive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0919936
UMLS CUI [1,2]
C0033554
no change of the PAH specific therapy within 3 weeks of the recruitment to the study
Descripción

no change of the PAH specific therapy soon after recruitment to the study

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2973725
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0205360
UMLS CUI [1,4]
C0332282
UMLS CUI [1,5]
C2603343
UMLS CUI [1,6]
C1512693
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy and lactation period
Descripción

pregnancy and lactation period

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
women of child bearing potential who do not use an effective and secure method for birth control
Descripción

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

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0332268
UMLS CUI [1,3]
C0700589
severe chronic kidney insufficiency (glomerular filtration rate <30), which will remain for more than 3 months
Descripción

persistent severe chronic kidney insufficiency (by GFR)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0205082
UMLS CUI [1,2]
C0403447
UMLS CUI [1,3]
C0449238
UMLS CUI [2]
C0017654
liver-insufficiency Child C
Descripción

liver insufficiency (Child-Pugh classification)

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1306571
UMLS CUI [2]
C4055253
life expectancy shorter than the course of the study (for example because of malignant disease)
Descripción

limited life expectancy (for example because of malignant disease)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0439801
UMLS CUI [2]
C0006826
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Similar models

Eligibility Criteria

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age >17
boolean
C0001779 (UMLS CUI [1])
pulmonary arterial hypertension (WHO grouping) starting a parenteral prostanoid-therapy
Item
pulmonary arterial hypertension (PAH) associated with WHO group 1 who start a parenteral prostanoid-therapy
boolean
C2973725 (UMLS CUI [1,1])
C4267671 (UMLS CUI [1,2])
C1704686 (UMLS CUI [2,1])
C0033554 (UMLS CUI [2,2])
C0678823 (UMLS CUI [2,3])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
prostanoid naive
Item
prostanoid naive
boolean
C0919936 (UMLS CUI [1,1])
C0033554 (UMLS CUI [1,2])
no change of the PAH specific therapy soon after recruitment to the study
Item
no change of the PAH specific therapy within 3 weeks of the recruitment to the study
boolean
C2973725 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0332282 (UMLS CUI [1,4])
C2603343 (UMLS CUI [1,5])
C1512693 (UMLS CUI [1,6])
Item Group
C0680251 (UMLS CUI)
pregnancy and lactation period
Item
pregnancy and lactation period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
women of child bearing potential who do not use an effective and secure method for birth control
Item
women of child bearing potential who do not use an effective and secure method for birth control
boolean
C3831118 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
persistent severe chronic kidney insufficiency (by GFR)
Item
severe chronic kidney insufficiency (glomerular filtration rate <30), which will remain for more than 3 months
boolean
C0205082 (UMLS CUI [1,1])
C0403447 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0017654 (UMLS CUI [2])
liver insufficiency (Child-Pugh classification)
Item
liver-insufficiency Child C
boolean
C1306571 (UMLS CUI [1])
C4055253 (UMLS CUI [2])
limited life expectancy (for example because of malignant disease)
Item
life expectancy shorter than the course of the study (for example because of malignant disease)
boolean
C0023671 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2])
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