ID

20078

Beschrijving

Atrial Fibrillation Ablation Pilot Study; ODM derived from: https://clinicaltrials.gov/show/NCT00744835

Link

https://clinicaltrials.gov/show/NCT00744835

Trefwoorden

  1. 05-02-17 05-02-17 -
Geüploaded op

5 februari 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00744835

Eligibility Atrial Fibrillation NCT00744835

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of symptomatic permanent atrial fibrillation
Beschrijving

Atrial fibrillation

Datatype

boolean

Alias
UMLS CUI [1]
C0004238
age between 18 and 70
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
willingness, ability and commitment to participate in baseline and follow-up evaluations for the full length of the study
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
structural heart disease of clinical significance
Beschrijving

Structural heart disease

Datatype

boolean

Alias
UMLS CUI [1]
C1290384
any prior ablation for atrial fibrillation
Beschrijving

Ablation for atrial fibrillation

Datatype

boolean

Alias
UMLS CUI [1]
C2702800
prior ablation for arrhythmias other than af within the past three months
Beschrijving

Ablation

Datatype

boolean

Alias
UMLS CUI [1]
C0547070
enrollment in any other ongoing arrhythmia study protocol
Beschrijving

Study Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
any ventricular tachyarrhythmias currently being treated where the arrhythmia or the management may interfere with this study
Beschrijving

Ventricular tachyarrhythmia

Datatype

boolean

Alias
UMLS CUI [1]
C0042514
active infection or sepsis
Beschrijving

Active infection or sepsis

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0243026
any history of cerebral vascular disease including stroke or tias
Beschrijving

Cerebral vascular disease

Datatype

boolean

Alias
UMLS CUI [1]
C0007820
pregnancy or lactation
Beschrijving

Gynaecological Status

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
left atrial thrombus at the time of ablation
Beschrijving

Left atrial thrombus

Datatype

boolean

Alias
UMLS CUI [1]
C3532827
untreatable allergy to contrast media
Beschrijving

Allergy to contrast media

Datatype

boolean

Alias
UMLS CUI [1]
C0570562
any diagnosis of af secondary to electrolyte imbalance, thyroid disease, or any other reversible or non-cardiovascular causes
Beschrijving

Electrolyte imbalance

Datatype

boolean

Alias
UMLS CUI [1]
C0342579
history of blood clotting (bleeding or thrombotic) abnormalities
Beschrijving

Bleeding disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0005779
known sensitivities to heparin or warfarin
Beschrijving

Sensitivities to heparin or warfarin

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0019134
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0043031
severe copd (identified by an fev1 < 1)
Beschrijving

FEV1

Datatype

boolean

Alias
UMLS CUI [1]
C0748133
severe comorbidity or poor general physical/mental health that, in the opinion of the investigator, will not allow the patient to be a good study candidate (i.e. other disease processes, mental capacity, substance abuse, shortened life expectance, etc.)
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Atrial Fibrillation NCT00744835

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Atrial fibrillation
Item
history of symptomatic permanent atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Age
Item
age between 18 and 70
boolean
C0001779 (UMLS CUI [1])
Informed consent
Item
willingness, ability and commitment to participate in baseline and follow-up evaluations for the full length of the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Structural heart disease
Item
structural heart disease of clinical significance
boolean
C1290384 (UMLS CUI [1])
Ablation for atrial fibrillation
Item
any prior ablation for atrial fibrillation
boolean
C2702800 (UMLS CUI [1])
Ablation
Item
prior ablation for arrhythmias other than af within the past three months
boolean
C0547070 (UMLS CUI [1])
Study Participation Status
Item
enrollment in any other ongoing arrhythmia study protocol
boolean
C2348568 (UMLS CUI [1])
Ventricular tachyarrhythmia
Item
any ventricular tachyarrhythmias currently being treated where the arrhythmia or the management may interfere with this study
boolean
C0042514 (UMLS CUI [1])
Active infection or sepsis
Item
active infection or sepsis
boolean
C0009450 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Cerebral vascular disease
Item
any history of cerebral vascular disease including stroke or tias
boolean
C0007820 (UMLS CUI [1])
Gynaecological Status
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Left atrial thrombus
Item
left atrial thrombus at the time of ablation
boolean
C3532827 (UMLS CUI [1])
Allergy to contrast media
Item
untreatable allergy to contrast media
boolean
C0570562 (UMLS CUI [1])
Electrolyte imbalance
Item
any diagnosis of af secondary to electrolyte imbalance, thyroid disease, or any other reversible or non-cardiovascular causes
boolean
C0342579 (UMLS CUI [1])
Bleeding disorders
Item
history of blood clotting (bleeding or thrombotic) abnormalities
boolean
C0005779 (UMLS CUI [1])
Sensitivities to heparin or warfarin
Item
known sensitivities to heparin or warfarin
boolean
C0020517 (UMLS CUI [1,1])
C0019134 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0043031 (UMLS CUI [2,2])
FEV1
Item
severe copd (identified by an fev1 < 1)
boolean
C0748133 (UMLS CUI [1])
Comorbidity
Item
severe comorbidity or poor general physical/mental health that, in the opinion of the investigator, will not allow the patient to be a good study candidate (i.e. other disease processes, mental capacity, substance abuse, shortened life expectance, etc.)
boolean
C0009488 (UMLS CUI [1])

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