ID

20078

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT00744835

Stichworte

  1. 05.02.17 05.02.17 -
Hochgeladen am

5. Februar 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00744835

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])

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