ID

29458

Descrizione

Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds; ODM derived from: https://clinicaltrials.gov/show/NCT00746356

collegamento

https://clinicaltrials.gov/show/NCT00746356

Keywords

versioni (1)
  1. 27/03/18 27/03/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

27 marzo 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Heart Failure NCT00746356

Inglese

Eligibility Heart Failure NCT00746356

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
have an approved indication, as outlined by american heart association/heart rhythm society (aha/hrs) guidelines, for implantation of an icd or crt-d for the treatment of life-threatening ventricular tachyarrhythmia(s) or heart failure, or undergo revision of their icd or crt-d system to replace the pulse generator.
Descrizione

Indication Implantation ICD | Indication Implantation of CRT-D | Therapeutic procedure Ventricular Tachycardia Life Threatening | Therapeutic procedure Heart failure Life Threatening | Revision ICD | Revision CRT-D System | Replacement Pulse Generator

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0021107
UMLS CUI [1,3]
C0162589
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C1135480
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0042514
UMLS CUI [3,3]
C2826244
UMLS CUI [4,1]
C0087111
UMLS CUI [4,2]
C0018801
UMLS CUI [4,3]
C2826244
UMLS CUI [5,1]
C1527075
UMLS CUI [5,2]
C0162589
UMLS CUI [6,1]
C1527075
UMLS CUI [6,2]
C1736558
UMLS CUI [7,1]
C0559956
UMLS CUI [7,2]
C1140627
have the ability to provide informed consent for study participation and be willing and able to comply with the prescribed follow-up tests and schedule of evaluations.
Descrizione

Informed Consent | Protocol Compliance

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
have a classification of status 1 for cardiac transplantation or consideration for transplantation over the next 3 months.
Descrizione

Heart Transplantation | Consideration Heart Transplantation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018823
UMLS CUI [2,1]
C0518609
UMLS CUI [2,2]
C0018823
have had a recent myocardial infarction, unstable angina or cardiac revascularization (percutaneous transluminal coronary angioplasty (ptca), stent or coronary artery bypass graft(cabg)) within 40 days of enrollment.
Descrizione

Myocardial Infarction | Angina, Unstable | Myocardial Revascularization | Percutaneous Transluminal Coronary Angioplasty | Stent | Coronary Artery Bypass Surgery

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0027056
UMLS CUI [4]
C2936173
UMLS CUI [5]
C0038257
UMLS CUI [6]
C0010055
have had a recent cerebrovascular accident (cva) or transient ischemic attack (tia) within 3 months of enrollment.
Descrizione

Cerebrovascular accident | Transient Ischemic Attack

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
are allergic to dexamethasone sodium phosphate (dsp).
Descrizione

Hypersensitivity Dexamethasone sodium phosphate

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0113286
be currently participating in a clinical investigation that includes an active treatment arm.
Descrizione

Study Subject Participation Status | Treatment Arm Included

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C1522541
UMLS CUI [2,2]
C0332257
be pregnant or are planning for pregnancy within 6 months following enrollment.
Descrizione

Pregnancy | Pregnancy, Planned

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
have a life expectancy of less than 6 months.
Descrizione

Life Expectancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023671
be less than 18 years of age.
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
Ritorna all'inizio della pagina

Similar models

Eligibility Heart Failure NCT00746356

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Indication Implantation ICD | Indication Implantation of CRT-D | Therapeutic procedure Ventricular Tachycardia Life Threatening | Therapeutic procedure Heart failure Life Threatening | Revision ICD | Revision CRT-D System | Replacement Pulse Generator
Item
have an approved indication, as outlined by american heart association/heart rhythm society (aha/hrs) guidelines, for implantation of an icd or crt-d for the treatment of life-threatening ventricular tachyarrhythmia(s) or heart failure, or undergo revision of their icd or crt-d system to replace the pulse generator.
boolean
C3146298 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C0162589 (UMLS CUI [1,3])
C3146298 (UMLS CUI [2,1])
C1135480 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C0042514 (UMLS CUI [3,2])
C2826244 (UMLS CUI [3,3])
C0087111 (UMLS CUI [4,1])
C0018801 (UMLS CUI [4,2])
C2826244 (UMLS CUI [4,3])
C1527075 (UMLS CUI [5,1])
C0162589 (UMLS CUI [5,2])
C1527075 (UMLS CUI [6,1])
C1736558 (UMLS CUI [6,2])
C0559956 (UMLS CUI [7,1])
C1140627 (UMLS CUI [7,2])
Informed Consent | Protocol Compliance
Item
have the ability to provide informed consent for study participation and be willing and able to comply with the prescribed follow-up tests and schedule of evaluations.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Heart Transplantation | Consideration Heart Transplantation
Item
have a classification of status 1 for cardiac transplantation or consideration for transplantation over the next 3 months.
boolean
C0018823 (UMLS CUI [1])
C0518609 (UMLS CUI [2,1])
C0018823 (UMLS CUI [2,2])
Myocardial Infarction | Angina, Unstable | Myocardial Revascularization | Percutaneous Transluminal Coronary Angioplasty | Stent | Coronary Artery Bypass Surgery
Item
have had a recent myocardial infarction, unstable angina or cardiac revascularization (percutaneous transluminal coronary angioplasty (ptca), stent or coronary artery bypass graft(cabg)) within 40 days of enrollment.
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0027056 (UMLS CUI [3])
C2936173 (UMLS CUI [4])
C0038257 (UMLS CUI [5])
C0010055 (UMLS CUI [6])
Cerebrovascular accident | Transient Ischemic Attack
Item
have had a recent cerebrovascular accident (cva) or transient ischemic attack (tia) within 3 months of enrollment.
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Hypersensitivity Dexamethasone sodium phosphate
Item
are allergic to dexamethasone sodium phosphate (dsp).
boolean
C0020517 (UMLS CUI [1,1])
C0113286 (UMLS CUI [1,2])
Study Subject Participation Status | Treatment Arm Included
Item
be currently participating in a clinical investigation that includes an active treatment arm.
boolean
C2348568 (UMLS CUI [1])
C1522541 (UMLS CUI [2,1])
C0332257 (UMLS CUI [2,2])
Pregnancy | Pregnancy, Planned
Item
be pregnant or are planning for pregnancy within 6 months following enrollment.
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Life Expectancy
Item
have a life expectancy of less than 6 months.
boolean
C0023671 (UMLS CUI [1])
Age
Item
be less than 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial