ID

38505

Beschrijving

NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing; ODM derived from: https://clinicaltrials.gov/show/NCT01969370

Link

https://clinicaltrials.gov/show/NCT01969370

Trefwoorden

  1. 22-10-19 22-10-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

22 oktober 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 Cancer NCT01969370

Eligibility Cancer NCT01969370

  1. StudyEvent: Eligibility
    1. Eligibility Cancer NCT01969370
Criteria
Beschrijving

Criteria

cancer
Beschrijving

Malignant Neoplasms

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
age of diagnosis
Beschrijving

Disease length

Datatype

boolean

Alias
UMLS CUI [1]
C0872146
presence of bilateral (or multiple) cancers
Beschrijving

Bilateral Carcinoma | Multiple malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C1332549
UMLS CUI [2]
C0346429
diagnosis of a rare type of cancer
Beschrijving

Malignant Neoplasm Type Rare

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C0522498
details of the family history
Beschrijving

Family history Details

Datatype

boolean

Alias
UMLS CUI [1,1]
C0241889
UMLS CUI [1,2]
C1522508
cardiovascular conditions
Beschrijving

Condition Cardiovascular

Datatype

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C3887460
certain clinical findings, such as prolonged qt interval on electrocardiogram.
Beschrijving

Prolonged QT interval Electrocardiogram

Datatype

boolean

Alias
UMLS CUI [1,1]
C0151878
UMLS CUI [1,2]
C0013798
presence of hypertrophic cardiomyopathy or aortic aneurysm
Beschrijving

Hypertrophic Cardiomyopathy | Aortic Aneurysm

Datatype

boolean

Alias
UMLS CUI [1]
C0007194
UMLS CUI [2]
C0003486
age of diagnosis
Beschrijving

Disease length

Datatype

boolean

Alias
UMLS CUI [1]
C0872146
presence of family history
Beschrijving

Family history

Datatype

boolean

Alias
UMLS CUI [1]
C0241889
pediatric neurodevelopmental disorders
Beschrijving

Neurodevelopmental Disorders Pediatric

Datatype

boolean

Alias
UMLS CUI [1,1]
C1535926
UMLS CUI [1,2]
C1521725
specific brain structural brain abnormalities
Beschrijving

Abnormality of brain morphology

Datatype

boolean

Alias
UMLS CUI [1]
C4021085
presence of certain seizure types
Beschrijving

Seizure Type

Datatype

boolean

Alias
UMLS CUI [1,1]
C0036572
UMLS CUI [1,2]
C0332307
dysmorphic features
Beschrijving

Dysmorphic features

Datatype

boolean

Alias
UMLS CUI [1]
C0432072

Similar models

Eligibility Cancer NCT01969370

  1. StudyEvent: Eligibility
    1. Eligibility Cancer NCT01969370
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Malignant Neoplasms
Item
cancer
boolean
C0006826 (UMLS CUI [1])
Disease length
Item
age of diagnosis
boolean
C0872146 (UMLS CUI [1])
Bilateral Carcinoma | Multiple malignancy
Item
presence of bilateral (or multiple) cancers
boolean
C1332549 (UMLS CUI [1])
C0346429 (UMLS CUI [2])
Malignant Neoplasm Type Rare
Item
diagnosis of a rare type of cancer
boolean
C0006826 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0522498 (UMLS CUI [1,3])
Family history Details
Item
details of the family history
boolean
C0241889 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
Condition Cardiovascular
Item
cardiovascular conditions
boolean
C0348080 (UMLS CUI [1,1])
C3887460 (UMLS CUI [1,2])
Prolonged QT interval Electrocardiogram
Item
certain clinical findings, such as prolonged qt interval on electrocardiogram.
boolean
C0151878 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
Hypertrophic Cardiomyopathy | Aortic Aneurysm
Item
presence of hypertrophic cardiomyopathy or aortic aneurysm
boolean
C0007194 (UMLS CUI [1])
C0003486 (UMLS CUI [2])
Disease length
Item
age of diagnosis
boolean
C0872146 (UMLS CUI [1])
Family history
Item
presence of family history
boolean
C0241889 (UMLS CUI [1])
Neurodevelopmental Disorders Pediatric
Item
pediatric neurodevelopmental disorders
boolean
C1535926 (UMLS CUI [1,1])
C1521725 (UMLS CUI [1,2])
Abnormality of brain morphology
Item
specific brain structural brain abnormalities
boolean
C4021085 (UMLS CUI [1])
Seizure Type
Item
presence of certain seizure types
boolean
C0036572 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Dysmorphic features
Item
dysmorphic features
boolean
C0432072 (UMLS CUI [1])

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