ID

33306

Description

Sequential Expansion of Comparative Effectiveness of Anticoagulants; ODM derived from: https://clinicaltrials.gov/show/NCT02081807

Lien

https://clinicaltrials.gov/show/NCT02081807

Mots-clés

Versions (1)
  1. 05/12/2018 05/12/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

5 décembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02081807

Anglais

Eligibility Atrial Fibrillation NCT02081807

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
a recorded diagnosis of atrial fibrillation.
Description

Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
initiation of anticoagulant medication (dabigatran (or other new oral anticoagulants as they become available) or warfarin).
Description

Anticoagulants | dabigatran | Oral anticoagulants | Warfarin

Type de données

boolean

Alias
UMLS CUI [1]
C0003280
UMLS CUI [2]
C2348066
UMLS CUI [3]
C0354604
UMLS CUI [4]
C0043031
at least 18 years of age on the date of anticoagulant initiation.
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
cha2ds2-vasc score at least 1
Description

CHA2DS2-VASc score

Type de données

boolean

Alias
UMLS CUI [1]
C4049268
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with missing or ambiguous age or sex information.
Description

Age Information Missing | Gender Information Missing | Age Information Indeterminate | Gender Information Indeterminate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1533716
UMLS CUI [1,3]
C1705492
UMLS CUI [2,1]
C0079399
UMLS CUI [2,2]
C1533716
UMLS CUI [2,3]
C1705492
UMLS CUI [3,1]
C0001779
UMLS CUI [3,2]
C1533716
UMLS CUI [3,3]
C0205258
UMLS CUI [4,1]
C0079399
UMLS CUI [4,2]
C1533716
UMLS CUI [4,3]
C0205258
patients with evidence of valvular disease.
Description

Valvular disease

Type de données

boolean

Alias
UMLS CUI [1]
C3258293
patients with less than 12 months enrolment preceding the date of anticoagulant initiation
Description

Enrollment Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0449238
patients with a dispensing of any oral anticoagulant during the 12 months preceding the date of anticoagulant initiation
Description

Oral anticoagulants Recently

Type de données

boolean

Alias
UMLS CUI [1,1]
C0354604
UMLS CUI [1,2]
C0332185
patients with a nursing home stay during the 12 months preceding the date of anticoagulant initiation
Description

Lives in a nursing home

Type de données

boolean

Alias
UMLS CUI [1]
C0425205
Retour au début de la page

Similar models

Eligibility Atrial Fibrillation NCT02081807

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation
Item
a recorded diagnosis of atrial fibrillation.
boolean
C0004238 (UMLS CUI [1])
Anticoagulants | dabigatran | Oral anticoagulants | Warfarin
Item
initiation of anticoagulant medication (dabigatran (or other new oral anticoagulants as they become available) or warfarin).
boolean
C0003280 (UMLS CUI [1])
C2348066 (UMLS CUI [2])
C0354604 (UMLS CUI [3])
C0043031 (UMLS CUI [4])
Age
Item
at least 18 years of age on the date of anticoagulant initiation.
boolean
C0001779 (UMLS CUI [1])
CHA2DS2-VASc score
Item
cha2ds2-vasc score at least 1
boolean
C4049268 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age Information Missing | Gender Information Missing | Age Information Indeterminate | Gender Information Indeterminate
Item
patients with missing or ambiguous age or sex information.
boolean
C0001779 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,3])
C0079399 (UMLS CUI [2,1])
C1533716 (UMLS CUI [2,2])
C1705492 (UMLS CUI [2,3])
C0001779 (UMLS CUI [3,1])
C1533716 (UMLS CUI [3,2])
C0205258 (UMLS CUI [3,3])
C0079399 (UMLS CUI [4,1])
C1533716 (UMLS CUI [4,2])
C0205258 (UMLS CUI [4,3])
Valvular disease
Item
patients with evidence of valvular disease.
boolean
C3258293 (UMLS CUI [1])
Enrollment Duration
Item
patients with less than 12 months enrolment preceding the date of anticoagulant initiation
boolean
C1516879 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Oral anticoagulants Recently
Item
patients with a dispensing of any oral anticoagulant during the 12 months preceding the date of anticoagulant initiation
boolean
C0354604 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Lives in a nursing home
Item
patients with a nursing home stay during the 12 months preceding the date of anticoagulant initiation
boolean
C0425205 (UMLS CUI [1])
Retour au début de la page 

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