ID

37556

Descrizione

Ventricular Wall Motion Characterization; ODM derived from: https://clinicaltrials.gov/show/NCT01629160

collegamento

https://clinicaltrials.gov/show/NCT01629160

Keywords

versioni (1)
  1. 07/08/19 07/08/19 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

7 agosto 2019

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 Atrial Fibrillation NCT01629160

Inglese

Eligibility Atrial Fibrillation NCT01629160

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
be in sinus rhythm
Descrizione

Sinus rhythm

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232201
have the ability to provide informed consent for study participation and be willing and able to comply with the clinical investigational plan described evaluations
Descrizione

Informed Consent | Compliance Evaluation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C1261322
be undergoing mapping and ablation that requires left heart access for either ventricular tachycardia (vt) or atrial fibrillation (af) according to hrs (heart rhythm society)/esc (european society of cardiology)/german national guidelines. the patient needs to have at least one of the following indications for left heart mapping and ablation to be included in the study: a) symptomatic sustained monomorphic vt (smvt), or b) frequent pvcs, non-sustained vt, or vt that is presumed to cause ventricular dysfunction, or c) bundle branch reentrant or interfascicular vts, or d) symptomatic af with indication for ablation per current hrs/esc/german national guidelines in a patient who is either 1) refractory or intolerant to at least one class 1 or class 3 antiarrhythmic medication, or 2) unable/unwilling to take antiarrhythmic drug therapy and chooses ablation as the first line of therapy
Descrizione

Mapping | Ablation | Left heart Access Ventricular Tachycardia | Left heart Access Atrial Fibrillation | Indication Mapping Left heart | Indication Ablation Left heart | Monomorphic ventricular tachycardia Symptomatic | Premature ventricular contractions Frequent | Non-sustained ventricular tachycardia | Ventricular Tachycardia Causing Ventricular Dysfunction | Bundle branch reentrant ventricular tachycardia | Ventricular Tachycardia interfascicular | ATRIAL FIBRILLATION SYMPTOMATIC | Indication Ablation | Unresponsive to Anti-Arrhythmia Agents Class Quantity | Intolerance to Anti-Arrhythmia Agents Class Quantity | Anti-Arrhythmia Agents Intake Unable | Anti-Arrhythmia Agents Intake Unwilling

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1283195
UMLS CUI [2]
C0547070
UMLS CUI [3,1]
C0225809
UMLS CUI [3,2]
C0444454
UMLS CUI [3,3]
C0042514
UMLS CUI [4,1]
C0225809
UMLS CUI [4,2]
C0444454
UMLS CUI [4,3]
C0004238
UMLS CUI [5,1]
C3146298
UMLS CUI [5,2]
C1283195
UMLS CUI [5,3]
C0225809
UMLS CUI [6,1]
C3146298
UMLS CUI [6,2]
C0547070
UMLS CUI [6,3]
C0225809
UMLS CUI [7,1]
C0344431
UMLS CUI [7,2]
C0231220
UMLS CUI [8,1]
C0151636
UMLS CUI [8,2]
C0332183
UMLS CUI [9]
C0750194
UMLS CUI [10,1]
C0042514
UMLS CUI [10,2]
C0678227
UMLS CUI [10,3]
C0242973
UMLS CUI [11]
C2711556
UMLS CUI [12,1]
C0042514
UMLS CUI [12,2]
C0228579
UMLS CUI [13]
C0741283
UMLS CUI [14,1]
C3146298
UMLS CUI [14,2]
C0547070
UMLS CUI [15,1]
C0205269
UMLS CUI [15,2]
C0003195
UMLS CUI [15,3]
C0456387
UMLS CUI [15,4]
C1265611
UMLS CUI [16,1]
C1744706
UMLS CUI [16,2]
C0003195
UMLS CUI [16,3]
C0456387
UMLS CUI [16,4]
C1265611
UMLS CUI [17,1]
C0003195
UMLS CUI [17,2]
C1512806
UMLS CUI [17,3]
C1299582
UMLS CUI [18,1]
C0003195
UMLS CUI [18,2]
C1512806
UMLS CUI [18,3]
C0558080
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
have permanent af
Descrizione

Permanent atrial fibrillation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2586056
exhibit cheyne-stokes respiration
Descrizione

Cheyne-Stokes Respiration

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0008039
have a recent myocardial infarction within 40 days prior to enrollment
Descrizione

Myocardial Infarction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0027051
have undergone cardiac surgery or coronary revascularization procedure within 3 months prior to enrollment or be scheduled for such procedures
Descrizione

Cardiac Surgery | Coronary revascularisation | Cardiac Surgery Scheduled | Coronary revascularisation Scheduled

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2]
C0877341
UMLS CUI [3,1]
C0018821
UMLS CUI [3,2]
C0205539
UMLS CUI [4,1]
C0877341
UMLS CUI [4,2]
C0205539
have had a recent cva or tia within 3 months prior to enrollment
Descrizione

Cerebrovascular accident | Transient Ischemic Attack

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
be less than 18 years of age
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
be pregnant
Descrizione

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
be currently participating in any other clinical investigation
Descrizione

Study Subject Participation Status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
Ritorna all'inizio della pagina

Similar models

Eligibility Atrial Fibrillation NCT01629160

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Sinus rhythm
Item
be in sinus rhythm
boolean
C0232201 (UMLS CUI [1])
Informed Consent | Compliance Evaluation
Item
have the ability to provide informed consent for study participation and be willing and able to comply with the clinical investigational plan described evaluations
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2,1])
C1261322 (UMLS CUI [2,2])
Mapping | Ablation | Left heart Access Ventricular Tachycardia | Left heart Access Atrial Fibrillation | Indication Mapping Left heart | Indication Ablation Left heart | Monomorphic ventricular tachycardia Symptomatic | Premature ventricular contractions Frequent | Non-sustained ventricular tachycardia | Ventricular Tachycardia Causing Ventricular Dysfunction | Bundle branch reentrant ventricular tachycardia | Ventricular Tachycardia interfascicular | ATRIAL FIBRILLATION SYMPTOMATIC | Indication Ablation | Unresponsive to Anti-Arrhythmia Agents Class Quantity | Intolerance to Anti-Arrhythmia Agents Class Quantity | Anti-Arrhythmia Agents Intake Unable | Anti-Arrhythmia Agents Intake Unwilling
Item
be undergoing mapping and ablation that requires left heart access for either ventricular tachycardia (vt) or atrial fibrillation (af) according to hrs (heart rhythm society)/esc (european society of cardiology)/german national guidelines. the patient needs to have at least one of the following indications for left heart mapping and ablation to be included in the study: a) symptomatic sustained monomorphic vt (smvt), or b) frequent pvcs, non-sustained vt, or vt that is presumed to cause ventricular dysfunction, or c) bundle branch reentrant or interfascicular vts, or d) symptomatic af with indication for ablation per current hrs/esc/german national guidelines in a patient who is either 1) refractory or intolerant to at least one class 1 or class 3 antiarrhythmic medication, or 2) unable/unwilling to take antiarrhythmic drug therapy and chooses ablation as the first line of therapy
boolean
C1283195 (UMLS CUI [1])
C0547070 (UMLS CUI [2])
C0225809 (UMLS CUI [3,1])
C0444454 (UMLS CUI [3,2])
C0042514 (UMLS CUI [3,3])
C0225809 (UMLS CUI [4,1])
C0444454 (UMLS CUI [4,2])
C0004238 (UMLS CUI [4,3])
C3146298 (UMLS CUI [5,1])
C1283195 (UMLS CUI [5,2])
C0225809 (UMLS CUI [5,3])
C3146298 (UMLS CUI [6,1])
C0547070 (UMLS CUI [6,2])
C0225809 (UMLS CUI [6,3])
C0344431 (UMLS CUI [7,1])
C0231220 (UMLS CUI [7,2])
C0151636 (UMLS CUI [8,1])
C0332183 (UMLS CUI [8,2])
C0750194 (UMLS CUI [9])
C0042514 (UMLS CUI [10,1])
C0678227 (UMLS CUI [10,2])
C0242973 (UMLS CUI [10,3])
C2711556 (UMLS CUI [11])
C0042514 (UMLS CUI [12,1])
C0228579 (UMLS CUI [12,2])
C0741283 (UMLS CUI [13])
C3146298 (UMLS CUI [14,1])
C0547070 (UMLS CUI [14,2])
C0205269 (UMLS CUI [15,1])
C0003195 (UMLS CUI [15,2])
C0456387 (UMLS CUI [15,3])
C1265611 (UMLS CUI [15,4])
C1744706 (UMLS CUI [16,1])
C0003195 (UMLS CUI [16,2])
C0456387 (UMLS CUI [16,3])
C1265611 (UMLS CUI [16,4])
C0003195 (UMLS CUI [17,1])
C1512806 (UMLS CUI [17,2])
C1299582 (UMLS CUI [17,3])
C0003195 (UMLS CUI [18,1])
C1512806 (UMLS CUI [18,2])
C0558080 (UMLS CUI [18,3])
Item Group
C0680251 (UMLS CUI)
Permanent atrial fibrillation
Item
have permanent af
boolean
C2586056 (UMLS CUI [1])
Cheyne-Stokes Respiration
Item
exhibit cheyne-stokes respiration
boolean
C0008039 (UMLS CUI [1])
Myocardial Infarction
Item
have a recent myocardial infarction within 40 days prior to enrollment
boolean
C0027051 (UMLS CUI [1])
Cardiac Surgery | Coronary revascularisation | Cardiac Surgery Scheduled | Coronary revascularisation Scheduled
Item
have undergone cardiac surgery or coronary revascularization procedure within 3 months prior to enrollment or be scheduled for such procedures
boolean
C0018821 (UMLS CUI [1])
C0877341 (UMLS CUI [2])
C0018821 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
C0877341 (UMLS CUI [4,1])
C0205539 (UMLS CUI [4,2])
Cerebrovascular accident | Transient Ischemic Attack
Item
have had a recent cva or tia within 3 months prior to enrollment
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Age
Item
be less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
be pregnant
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status
Item
be currently participating in any other clinical investigation
boolean
C2348568 (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