Informatie:
Fout:
ID
34131
Beschrijving
Atrial Fibrillation/Flutter Outcome Risk Determination; ODM derived from: https://clinicaltrials.gov/show/NCT01138644
Link
https://clinicaltrials.gov/show/NCT01138644
Trefwoorden
Versies (1)
- 14-01-19 14-01-19 -
Houder van rechten
see on clinicaltrials.gov
Geüploaded op
14 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01138644
Eligibility Atrial Fibrillation NCT01138644
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01138644
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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
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