ID

23472

Description

Surgical or Catheter Ablation of Lone Atrial Fibrillation (AF) Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00703157

Link

https://clinicaltrials.gov/show/NCT00703157

Keywords

Versions (1)
  1. 7/6/17 7/6/17 -
Uploaded on

July 6, 2017

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Atrial Fibrillation NCT00703157

English

Eligibility Atrial Fibrillation NCT00703157

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has documented paroxysmal af as defined by the acc/aha/esc guidelines
Description

Paroxysmal atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C0235480
minimal one documented af episode in the last 6 months
Description

Atrial Fibrillation Episode Quantity Minimum

Data type

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0332189
UMLS CUI [1,3]
C1265611
UMLS CUI [1,4]
C1524031
refractory to minimal two class i or iii anti-arrhythmic drug
Description

Anti-Arrhythmia Agents refractory | Anti-Arrhythmia Agents Class Quantity Minimum

Data type

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0205269
UMLS CUI [2,1]
C0003195
UMLS CUI [2,2]
C0456387
UMLS CUI [2,3]
C1265611
UMLS CUI [2,4]
C1524031
age > 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
signed and dated the patient informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patient can tolerate anti-coagulation therapy (warfarin/coumadin)
Description

Anticoagulation Therapy Receive Ability | Warfarin | Coumadin

Data type

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0085732
UMLS CUI [2]
C0043031
UMLS CUI [3]
C0699129
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient has a structural heart disease
Description

Structural disorder of heart

Data type

boolean

Alias
UMLS CUI [1]
C1290384
ejection fraction < 40 %
Description

Cardiac ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0232174
echocardiographic evidence for a left atrium > 45 mm (parasternal axis)
Description

Left atrium Size | Echocardiography Axis Parasternal

Data type

boolean

Alias
UMLS CUI [1,1]
C0225860
UMLS CUI [1,2]
C0456389
UMLS CUI [2,1]
C0013516
UMLS CUI [2,2]
C1522496
UMLS CUI [2,3]
C0442146
patients on amiodarone, or patients known to be intolerant for amiodarone
Description

Amiodarone | Intolerance to Amiodarone

Data type

boolean

Alias
UMLS CUI [1]
C0002598
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0002598
dextrocardia, current endocarditis, systemic infection, renal failure
Description

Dextrocardia | Endocarditis | Sepsis | Kidney Failure

Data type

boolean

Alias
UMLS CUI [1]
C0011813
UMLS CUI [2]
C0014118
UMLS CUI [3]
C0243026
UMLS CUI [4]
C0035078
patient has known cerebrovascular disease, including a history of stroke, cva or tia
Description

Cerebrovascular Disorders | Cerebrovascular accident | Transient Ischemic Attack

Data type

boolean

Alias
UMLS CUI [1]
C0007820
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0007787
pregnancy at enrolment; or planned pregnancy within the follow up period
Description

Pregnancy | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
patient has a life expectancy less than 1 year
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
the subject is participating in another device or drug study
Description

Study Subject Participation Status | Investigational Medical Device | Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C2346570
UMLS CUI [3]
C0013230
the patient is unable and/or unwilling to cooperate with study procedures or required follow up visits
Description

Protocol Compliance Unable | Protocol Compliance Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C0558080
echocardiographic (tte) evidence for presence of left atrial thrombus
Description

Thrombus of left atrium Transthoracic echocardiography

Data type

boolean

Alias
UMLS CUI [1,1]
C3532827
UMLS CUI [1,2]
C0430462
previous (cardio-) thoracic surgery
Description

Thoracic Surgical Procedures | Cardiothoracic surgery

Data type

boolean

Alias
UMLS CUI [1]
C0524832
UMLS CUI [2]
C2242990
previous left atrial ablation
Description

Left atrium Ablation

Data type

boolean

Alias
UMLS CUI [1,1]
C0225860
UMLS CUI [1,2]
C0547070
patients with permanent or persistent af
Description

Permanent atrial fibrillation | Persistent atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C2586056
UMLS CUI [2]
C2585653
Back to the top of the page

Similar models

Eligibility Atrial Fibrillation NCT00703157

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Paroxysmal atrial fibrillation
Item
patient has documented paroxysmal af as defined by the acc/aha/esc guidelines
boolean
C0235480 (UMLS CUI [1])
Atrial Fibrillation Episode Quantity Minimum
Item
minimal one documented af episode in the last 6 months
boolean
C0004238 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1524031 (UMLS CUI [1,4])
Anti-Arrhythmia Agents refractory | Anti-Arrhythmia Agents Class Quantity Minimum
Item
refractory to minimal two class i or iii anti-arrhythmic drug
boolean
C0003195 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0003195 (UMLS CUI [2,1])
C0456387 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C1524031 (UMLS CUI [2,4])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
signed and dated the patient informed consent.
boolean
C0021430 (UMLS CUI [1])
Anticoagulation Therapy Receive Ability | Warfarin | Coumadin
Item
patient can tolerate anti-coagulation therapy (warfarin/coumadin)
boolean
C0003281 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0043031 (UMLS CUI [2])
C0699129 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Structural disorder of heart
Item
patient has a structural heart disease
boolean
C1290384 (UMLS CUI [1])
Cardiac ejection fraction
Item
ejection fraction < 40 %
boolean
C0232174 (UMLS CUI [1])
Left atrium Size | Echocardiography Axis Parasternal
Item
echocardiographic evidence for a left atrium > 45 mm (parasternal axis)
boolean
C0225860 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
C0013516 (UMLS CUI [2,1])
C1522496 (UMLS CUI [2,2])
C0442146 (UMLS CUI [2,3])
Amiodarone | Intolerance to Amiodarone
Item
patients on amiodarone, or patients known to be intolerant for amiodarone
boolean
C0002598 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0002598 (UMLS CUI [2,2])
Dextrocardia | Endocarditis | Sepsis | Kidney Failure
Item
dextrocardia, current endocarditis, systemic infection, renal failure
boolean
C0011813 (UMLS CUI [1])
C0014118 (UMLS CUI [2])
C0243026 (UMLS CUI [3])
C0035078 (UMLS CUI [4])
Cerebrovascular Disorders | Cerebrovascular accident | Transient Ischemic Attack
Item
patient has known cerebrovascular disease, including a history of stroke, cva or tia
boolean
C0007820 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
Pregnancy | Pregnancy, Planned
Item
pregnancy at enrolment; or planned pregnancy within the follow up period
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Life Expectancy
Item
patient has a life expectancy less than 1 year
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status | Investigational Medical Device | Investigational New Drugs
Item
the subject is participating in another device or drug study
boolean
C2348568 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
Protocol Compliance Unable | Protocol Compliance Unwilling
Item
the patient is unable and/or unwilling to cooperate with study procedures or required follow up visits
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Thrombus of left atrium Transthoracic echocardiography
Item
echocardiographic (tte) evidence for presence of left atrial thrombus
boolean
C3532827 (UMLS CUI [1,1])
C0430462 (UMLS CUI [1,2])
Thoracic Surgical Procedures | Cardiothoracic surgery
Item
previous (cardio-) thoracic surgery
boolean
C0524832 (UMLS CUI [1])
C2242990 (UMLS CUI [2])
Left atrium Ablation
Item
previous left atrial ablation
boolean
C0225860 (UMLS CUI [1,1])
C0547070 (UMLS CUI [1,2])
Permanent atrial fibrillation | Persistent atrial fibrillation
Item
patients with permanent or persistent af
boolean
C2586056 (UMLS CUI [1])
C2585653 (UMLS CUI [2])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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