Information: Detta är inte den senaste versionen av datamodellen. Du hittar en versionsöversikt till vänster under versioner. Den senaste versionen hittar du här.
Information:
Fel:
ID
33282
Beskrivning
Carvedilol for Prevention of Paroxysmal Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01608893
Länk
https://clinicaltrials.gov/show/NCT01608893
Nyckelord
Versioner (2)
- 2018-12-04 2018-12-04 -
- 2018-12-04 2018-12-04 -
Rättsinnehavare
See4 clinicaltrials.gov
Uppladdad den
4 december 2018
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Atrial Fibrillation NCT01608893
Eligibility Atrial Fibrillation NCT01608893
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01608893
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Sinus rhythm
Item
must be in sinus rhythm at enrollment
boolean
C0232201 (UMLS CUI [1])
Paroxysmal atrial fibrillation Symptomatic ECG | Episode Quantity Duration Period
Item
ecg documented symptomatic paf (> 2 episodes of > 15minutes duration over a 6 month period)
boolean
C0235480 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C1623258 (UMLS CUI [1,3])
C0332189 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
C1948053 (UMLS CUI [2,4])
C0231220 (UMLS CUI [1,2])
C1623258 (UMLS CUI [1,3])
C0332189 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
C1948053 (UMLS CUI [2,4])
Atrial Fibrillation Causes Reversible
Item
af due to reversible causes
boolean
C0004238 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0205343 (UMLS CUI [1,3])
C0015127 (UMLS CUI [1,2])
C0205343 (UMLS CUI [1,3])
Medical contraindication Adrenergic beta-1 Receptor Antagonists | Adverse reactions Adrenergic beta-1 Receptor Antagonists
Item
contraindication or previous significant adverse reaction to beta blocker therapy
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0559546 (UMLS CUI [2,1])
C0304516 (UMLS CUI [2,2])
C0304516 (UMLS CUI [1,2])
C0559546 (UMLS CUI [2,1])
C0304516 (UMLS CUI [2,2])
Persistent atrial fibrillation
Item
persistent af
boolean
C2585653 (UMLS CUI [1])
Congestive heart failure New York Heart Association Classification
Item
nyha class ii or greater chf
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction
Item
lvef < or = 35%
boolean
C0428772 (UMLS CUI [1])
Life Expectancy
Item
life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
Isolation Geographic
Item
geographic isolation
boolean
C0205409 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
C1517526 (UMLS CUI [1,2])
Informed Consent Unable
Item
unable to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])