ID

37529

Description

CPVI Plus Renal Sympathetic Modification Versus CPVI Alone for AF（Atrial Fibrillation） Ablation; ODM derived from: https://clinicaltrials.gov/show/NCT01686542

Lien

https://clinicaltrials.gov/show/NCT01686542

Mots-clés

Versions (1)
  1. 05/08/2019 05/08/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

5 août 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01686542

Anglais

Eligibility Atrial Fibrillation NCT01686542

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
• ≥ 18 years old, and ≤ 75 years old of age
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
more than half a year history of atrial fibrillation, no matter paroxysmal or persistent, with clinical symptom or ecg proved
Description

Atrial Fibrillation Disease length Symptoms | Atrial Fibrillation Disease length Electrocardiography | Paroxysmal atrial fibrillation | Persistent atrial fibrillation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
UMLS CUI [1,3]
C1457887
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0872146
UMLS CUI [2,3]
C1623258
UMLS CUI [3]
C0235480
UMLS CUI [4]
C2585653
be ineffective to at least one kind of anti-arrhythmic drugs treatment
Description

Anti-Arrhythmia Agents Kind Quantity ineffective

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C1265611
UMLS CUI [1,4]
C3242229
echocardiography has done to except structural heart diseases such as congenital, valvular heart diseases and kinds of cardiomyopathy
Description

Echocardiography Excludes Structural disorder of heart | Echocardiography Excludes Congenital heart disease | Echocardiography Excludes Heart valve disease | Echocardiography Excludes Cardiomyopathy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013516
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C1290384
UMLS CUI [2,1]
C0013516
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C0152021
UMLS CUI [3,1]
C0013516
UMLS CUI [3,2]
C0332196
UMLS CUI [3,3]
C0018824
UMLS CUI [4,1]
C0013516
UMLS CUI [4,2]
C0332196
UMLS CUI [4,3]
C0878544
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
Description

Estimated Glomerular Filtration Rate

Type de données

boolean

Alias
UMLS CUI [1]
C3811844
is competent and willing to provide written, informed consent to participate in this clinical study
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
• transesophageal echocardiography found thrombus in left atrial appendage
Description

Thrombus Left Atrial Appendage Transesophageal Echocardiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087086
UMLS CUI [1,2]
C4284918
UMLS CUI [1,3]
C0206054
past history of atrial fibrillation surgical maze procedure
Description

Surgical Maze Procedure Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1,1]
C3272262
UMLS CUI [1,2]
C0004238
estimated glomerular filtration rate (egfr) of < 45ml/min
Description

Estimated Glomerular Filtration Rate

Type de données

boolean

Alias
UMLS CUI [1]
C3811844
has the history of renal restenosis or renal stents implantation
Description

Restenosis renal | Renal artery stent placement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0333186
UMLS CUI [1,2]
C0022646
UMLS CUI [2]
C1609503
has experienced ami（acute myocardial infarction） (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
Description

Myocardial Infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0017181
patients with sick sinus syndrome
Description

Sick Sinus Syndrome

Type de données

boolean

Alias
UMLS CUI [1]
C0037052
pregnant women
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
mental disorders
Description

Mental disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0004936
patients that have allergy to contrast agent
Description

Contrast media allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0570562
patients that do not go with follow-up
Description

Compliance Follow-up Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C3274571
UMLS CUI [1,3]
C0332268
others such as researcher considers it is not appropriate to be included into the study
Description

Study Subject Participation Status Inappropriate

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
Retour au début de la page

Similar models

Eligibility Atrial Fibrillation NCT01686542

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
• ≥ 18 years old, and ≤ 75 years old of age
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation Disease length Symptoms | Atrial Fibrillation Disease length Electrocardiography | Paroxysmal atrial fibrillation | Persistent atrial fibrillation
Item
more than half a year history of atrial fibrillation, no matter paroxysmal or persistent, with clinical symptom or ecg proved
boolean
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C1623258 (UMLS CUI [2,3])
C0235480 (UMLS CUI [3])
C2585653 (UMLS CUI [4])
Anti-Arrhythmia Agents Kind Quantity ineffective
Item
be ineffective to at least one kind of anti-arrhythmic drugs treatment
boolean
C0003195 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C3242229 (UMLS CUI [1,4])
Echocardiography Excludes Structural disorder of heart | Echocardiography Excludes Congenital heart disease | Echocardiography Excludes Heart valve disease | Echocardiography Excludes Cardiomyopathy
Item
echocardiography has done to except structural heart diseases such as congenital, valvular heart diseases and kinds of cardiomyopathy
boolean
C0013516 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C1290384 (UMLS CUI [1,3])
C0013516 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0152021 (UMLS CUI [2,3])
C0013516 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0018824 (UMLS CUI [3,3])
C0013516 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])
C0878544 (UMLS CUI [4,3])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
boolean
C3811844 (UMLS CUI [1])
Informed Consent
Item
is competent and willing to provide written, informed consent to participate in this clinical study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Thrombus Left Atrial Appendage Transesophageal Echocardiography
Item
• transesophageal echocardiography found thrombus in left atrial appendage
boolean
C0087086 (UMLS CUI [1,1])
C4284918 (UMLS CUI [1,2])
C0206054 (UMLS CUI [1,3])
Surgical Maze Procedure Atrial Fibrillation
Item
past history of atrial fibrillation surgical maze procedure
boolean
C3272262 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of < 45ml/min
boolean
C3811844 (UMLS CUI [1])
Restenosis renal | Renal artery stent placement
Item
has the history of renal restenosis or renal stents implantation
boolean
C0333186 (UMLS CUI [1,1])
C0022646 (UMLS CUI [1,2])
C1609503 (UMLS CUI [2])
Myocardial Infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage
Item
has experienced ami（acute myocardial infarction） (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0017181 (UMLS CUI [4])
Sick Sinus Syndrome
Item
patients with sick sinus syndrome
boolean
C0037052 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Mental disorders
Item
mental disorders
boolean
C0004936 (UMLS CUI [1])
Contrast media allergy
Item
patients that have allergy to contrast agent
boolean
C0570562 (UMLS CUI [1])
Compliance Follow-up Lacking
Item
patients that do not go with follow-up
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Study Subject Participation Status Inappropriate
Item
others such as researcher considers it is not appropriate to be included into the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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