ID

34544

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02207868

Nyckelord

  1. 2019-01-19 2019-01-19 -
  2. 2019-05-22 2019-05-22 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

19 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Pulmonary Arterial Hypertension NCT02207868

Eligibility Pulmonary Arterial Hypertension NCT02207868

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
age >17
Beskrivning

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

written informed consent
Beskrivning

ID.3

Datatyp

boolean

prostanoid naive
Beskrivning

ID.4

Datatyp

boolean

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

ID.5

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy and lactation period
Beskrivning

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

liver-insufficiency child c
Beskrivning

ID.9

Datatyp

boolean

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

ID.10

Datatyp

boolean

Similar models

Eligibility Pulmonary Arterial Hypertension NCT02207868

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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