ID

34131

Description

Atrial Fibrillation/Flutter Outcome Risk Determination; ODM derived from: https://clinicaltrials.gov/show/NCT01138644

Lien

https://clinicaltrials.gov/show/NCT01138644

Mots-clés

  1. 14/01/2019 14/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

14 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Atrial Fibrillation NCT01138644

Eligibility Atrial Fibrillation NCT01138644

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ed patients 18 years and older
Description

ID.1

Type de données

boolean

provide informed consent
Description

ID.2

Type de données

boolean

have a documented diagnosis of af or atrial flutter on electrocardiogram or rhythm strip from an ed, prehospital provider or outside medical facility on day of enrollment.
Description

ID.3

Type de données

boolean

present with signs (tachycardia, dyspnea) or symptoms (palpitations, chest pain, shortness of breath, weakness, lightheadedness, pre-syncope, or syncope) consistent with primary symptomatic af
Description

ID.4

Type de données

boolean

patients whose primary complaint is not directly related to their af diagnosis (e.g. evaluation for febrile illness, gastrointestinal complaint, injury) but have a secondary complaint consistent with symptomatic af that requires ed evaluation (e.g. new af diagnosis, af associated with inadequate rate control (defined as resting heart rate greater than 100bon), af associated with heart failure symptoms, af in the setting of cva or tia, af associated with other thromboembolic complications).
Description

ID.5

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are under the age of 18
Description

ID.6

Type de données

boolean

previously enrolled patients
Description

ID.7

Type de données

boolean

ed patients who present with complaints unrelated to their af (e.g. sprained ankle,pharyngitis) and have adequately rate (<100 bpm at rest) or rhythm controlled-af.
Description

ID.8

Type de données

boolean

Similar models

Eligibility Atrial Fibrillation NCT01138644

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
ed patients 18 years and older
boolean
ID.2
Item
provide informed consent
boolean
ID.3
Item
have a documented diagnosis of af or atrial flutter on electrocardiogram or rhythm strip from an ed, prehospital provider or outside medical facility on day of enrollment.
boolean
ID.4
Item
present with signs (tachycardia, dyspnea) or symptoms (palpitations, chest pain, shortness of breath, weakness, lightheadedness, pre-syncope, or syncope) consistent with primary symptomatic af
boolean
ID.5
Item
patients whose primary complaint is not directly related to their af diagnosis (e.g. evaluation for febrile illness, gastrointestinal complaint, injury) but have a secondary complaint consistent with symptomatic af that requires ed evaluation (e.g. new af diagnosis, af associated with inadequate rate control (defined as resting heart rate greater than 100bon), af associated with heart failure symptoms, af in the setting of cva or tia, af associated with other thromboembolic complications).
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients who are under the age of 18
boolean
ID.7
Item
previously enrolled patients
boolean
ID.8
Item
ed patients who present with complaints unrelated to their af (e.g. sprained ankle,pharyngitis) and have adequately rate (<100 bpm at rest) or rhythm controlled-af.
boolean

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