Eligibility Atrial Fibrillation NCT00744835

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of symptomatic permanent atrial fibrillation
Beschreibung

Atrial fibrillation

Datentyp

boolean

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

Age

Datentyp

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
Beschreibung

Informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
structural heart disease of clinical significance
Beschreibung

Structural heart disease

Datentyp

boolean

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

Ablation for atrial fibrillation

Datentyp

boolean

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

Ablation

Datentyp

boolean

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

Study Participation Status

Datentyp

boolean

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

Ventricular tachyarrhythmia

Datentyp

boolean

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

Active infection or sepsis

Datentyp

boolean

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

Cerebral vascular disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0007820
pregnancy or lactation
Beschreibung

Gynaecological Status

Datentyp

boolean

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

Left atrial thrombus

Datentyp

boolean

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

Allergy to contrast media

Datentyp

boolean

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

Electrolyte imbalance

Datentyp

boolean

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

Bleeding disorders

Datentyp

boolean

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

Sensitivities to heparin or warfarin

Datentyp

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)
Beschreibung

FEV1

Datentyp

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.)
Beschreibung

Comorbidity

Datentyp

boolean

Alias
UMLS CUI [1]
C0009488

Ähnliche Modelle

Eligibility Atrial Fibrillation NCT00744835

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])