Informations:
Erreur:
ID
39401
Description
INvestigation on Routine Follow-up in CONgestive HearT FAilure Patients With Remotely Monitored Implanted Cardioverter Defibrillators (ICD) SysTems; ODM derived from: https://clinicaltrials.gov/show/NCT01200381
Lien
https://clinicaltrials.gov/show/NCT01200381
Mots-clés
Versions (1)
- 08/01/2020 08/01/2020 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
8 janvier 2020
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Heart Failure NCT01200381
Eligibility Heart Failure NCT01200381
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT01200381
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Indication ICD Placement | Indication Implantation of CRT-D
Item
indication for implantation (new, boxchange, upgrade) of icd/ crt-d
boolean
C3146298 (UMLS CUI [1,1])
C2825184 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C1135480 (UMLS CUI [2,2])
C2825184 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C1135480 (UMLS CUI [2,2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Cardiac ejection fraction
Item
ejection fraction <= 35%
boolean
C0232174 (UMLS CUI [1])
New York Heart Association Classification
Item
new york heart association (nyha) class i-iii
boolean
C1275491 (UMLS CUI [1])
Age
Item
age >=18 and <=80 years
boolean
C0001779 (UMLS CUI [1])
Availability of Mobile Phone Network
Item
in patient's home environment sufficient infrastructure (analog phone line or sufficient strength of gsm (global system for mobile communication) mobile phone network) for running a merlin@home transmitter is available
boolean
C0470187 (UMLS CUI [1,1])
C1136360 (UMLS CUI [1,2])
C1882071 (UMLS CUI [1,3])
C1136360 (UMLS CUI [1,2])
C1882071 (UMLS CUI [1,3])
Complete atrioventricular block | Mobitz type II atrioventricular block
Item
arterio ventricular (av) block iii / av block ii type mobitz
boolean
C0151517 (UMLS CUI [1])
C0155700 (UMLS CUI [2])
C0155700 (UMLS CUI [2])
Renal Insufficiency Severe
Item
severe renal insufficiency
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Coronary angiography
Item
coronary angiology intervention within previous 3 months
boolean
C0085532 (UMLS CUI [1])
Myocardial Infarction
Item
myocardial infarction within previous month
boolean
C0027051 (UMLS CUI [1])
Life Expectancy
Item
life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
Data Quality Poor Expected | Poor compliance Expected
Item
expected poor data quality / compliance
boolean
C0242483 (UMLS CUI [1,1])
C0542537 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,3])
C0032646 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
C0542537 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,3])
C0032646 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial Treatment Arm
Item
patient is already participating to another study with active therapy arm
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C1522541 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,1])
C1522541 (UMLS CUI [2,2])