Information:
Fel:
ID
34379
Beskrivning
Educational Training Influence in Patients With PAH(Pulmonary Artery Hypertension) on Inhaled Ventavis Treatment Adherence Evaluated Trough INSIGHT System; ODM derived from: https://clinicaltrials.gov/show/NCT01468545
Länk
https://clinicaltrials.gov/show/NCT01468545
Nyckelord
Versioner (1)
- 2019-01-17 2019-01-17 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
17 januari 2019
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Pulmonary Arterial Hypertension NCT01468545
Eligibility Pulmonary Arterial Hypertension NCT01468545
- StudyEvent: Eligibility
Similar models
Eligibility Pulmonary Arterial Hypertension NCT01468545
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
male or female patients > 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Pulmonary Hypertension New York Heart Association Classification | Ventavis | Other Coding
Item
patients in new york heart association (nyha) functional class ii-iv pulmonary hypertension who are treated with ventavis at least three months before and who use-neb ® aad ® system.
boolean
C0020542 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1541936 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
C1275491 (UMLS CUI [1,2])
C1541936 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
Informed Consent
Item
patients who accepted participation in the study and sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Compliance behavior Instructions | Study Subject Participation Status Completion of clinical trial
Item
patients with ability to understand and follow the instructions and are able to participate for the duration of the study.
boolean
C1321605 (UMLS CUI [1,1])
C2051542 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C2732579 (UMLS CUI [2,2])
C2051542 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C2732579 (UMLS CUI [2,2])
Severe cognitive impairment
Item
patients with severe cognitive impairment.
boolean
C3554639 (UMLS CUI [1])
Unstable status Geographic | Follow-up Unsuccessful
Item
geographically unstable patients who can not be followed during the 12 month study.
boolean
C0443343 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
C1517526 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Life Expectancy
Item
patients who have a life expectancy of at least 12 months.
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status
Item
patients who are participating in another study at the time of inclusion. .
boolean
C2348568 (UMLS CUI [1])