Informations:
Erreur:
ID
39460
Description
Feasibility Trial of the DC Devices Interatrial Septal Device (IASD) System; ODM derived from: https://clinicaltrials.gov/show/NCT01570517
Lien
https://clinicaltrials.gov/show/NCT01570517
Mots-clés
Versions (1)
- 12/01/2020 12/01/2020 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
12 janvier 2020
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
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Eligibility Heart Failure NCT01570517
Eligibility Heart Failure NCT01570517
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT01570517
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Heart failure with preserved ejection fraction [HFpEF]
Item
clinical diagnosis of hfpef
boolean
C4509226 (UMLS CUI [1])
Cardiac ejection fraction
Item
ejection fraction of at least 45%
boolean
C0232174 (UMLS CUI [1])
HFpEF Imaging | HFpEF Evidence Hemodynamic
Item
imaging and hemodynamic evidence of hfpef
boolean
C4509226 (UMLS CUI [1,1])
C0011923 (UMLS CUI [1,2])
C4509226 (UMLS CUI [2,1])
C3887511 (UMLS CUI [2,2])
C0019010 (UMLS CUI [2,3])
C0011923 (UMLS CUI [1,2])
C4509226 (UMLS CUI [2,1])
C3887511 (UMLS CUI [2,2])
C0019010 (UMLS CUI [2,3])
Impaired exercise tolerance
Item
history of exercise intolerance
boolean
C0424551 (UMLS CUI [1])
Symptomatic | Disease Management Optimal
Item
symptomatic despite optimal medical management
boolean
C0231220 (UMLS CUI [1])
C0376636 (UMLS CUI [2,1])
C2698651 (UMLS CUI [2,2])
C0376636 (UMLS CUI [2,1])
C2698651 (UMLS CUI [2,2])
Informed Consent
Item
signed study specific informed consent
boolean
C0021430 (UMLS CUI [1])
Thromboembolism
Item
history of thromboembolic events
boolean
C0040038 (UMLS CUI [1])
Structural disorder of heart | Coronary Artery Disease
Item
significant structural heart disease or coronary artery disease
boolean
C1290384 (UMLS CUI [1])
C1956346 (UMLS CUI [2])
C1956346 (UMLS CUI [2])
Medical contraindication Investigational New Drugs
Item
contraindicated to study required medication
boolean
C1301624 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Ventricular Dysfunction, Right
Item
right ventricular dysfunction
boolean
C0242707 (UMLS CUI [1])
Restrictive lung disease Moderate | Obstructive Lung Disease Moderate | Restrictive lung disease Severe | Obstructive Lung Disease Severe
Item
history of greater than mild restrictive or obstructive lung disease
boolean
C0085581 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0600260 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C0085581 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0600260 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0205081 (UMLS CUI [1,2])
C0600260 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C0085581 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0600260 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Life Expectancy | Absence Etiology Cardiovascular
Item
life expectancy less than one year for non-cardiovascular reasons
boolean
C0023671 (UMLS CUI [1])
C0332197 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C3887460 (UMLS CUI [2,3])
C0332197 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C3887460 (UMLS CUI [2,3])
Hypersensitivity Implant material | Hypersensitivity Suspected Implant material
Item
known or suspected allergy to implant material
boolean
C0020517 (UMLS CUI [1,1])
C0440216 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0440216 (UMLS CUI [2,3])
C0440216 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0440216 (UMLS CUI [2,3])
Childbearing Potential
Item
fertile women
boolean
C3831118 (UMLS CUI [1])