ID

34231

Beschrijving

COmparison and Modification in Neointimal Pattern Assessed by Optical Coherence Tomography With High Versus Moderate Efficacy Statin Treatment After Drug Eluting Stent Implantation: COMPASS Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02155530

Link

https://clinicaltrials.gov/show/NCT02155530

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Coronary Artery Disease NCT02155530

Eligibility Coronary Artery Disease NCT02155530

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is ≥ 20 years old
Beschrijving

ID.1

Datatype

boolean

patients who received oct related to clinical needs or the end point of other study
Beschrijving

ID.2

Datatype

boolean

patients who received des within 1 year before oct evaluation
Beschrijving

ID.3

Datatype

boolean

patients with homogenous or hetero neointimal pattern by oct
Beschrijving

ID.4

Datatype

boolean

non-statin user and moderate or low efficacy statin user
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
refuse to participate
Beschrijving

ID.6

Datatype

boolean

contraindication to statin treatment
Beschrijving

ID.7

Datatype

boolean

women with current or potential childbearing
Beschrijving

ID.8

Datatype

boolean

life expectancy <1 year
Beschrijving

ID.9

Datatype

boolean

high efficacy statin user (atorvastatin 80mg or rosuvastatin 20mg)
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Coronary Artery Disease NCT02155530

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient is ≥ 20 years old
boolean
ID.2
Item
patients who received oct related to clinical needs or the end point of other study
boolean
ID.3
Item
patients who received des within 1 year before oct evaluation
boolean
ID.4
Item
patients with homogenous or hetero neointimal pattern by oct
boolean
ID.5
Item
non-statin user and moderate or low efficacy statin user
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
refuse to participate
boolean
ID.7
Item
contraindication to statin treatment
boolean
ID.8
Item
women with current or potential childbearing
boolean
ID.9
Item
life expectancy <1 year
boolean
ID.10
Item
high efficacy statin user (atorvastatin 80mg or rosuvastatin 20mg)
boolean

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial