ID

33839

Descripción

Genetic Testing to Understand and Address Renal Disease Disparities; ODM derived from: https://clinicaltrials.gov/show/NCT02234063

Link

https://clinicaltrials.gov/show/NCT02234063

Palabras clave

  1. 3/1/19 3/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

3 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Hypertension NCT02234063

Eligibility Hypertension NCT02234063

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
ages18-65
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
self-identifies as black/african american
Descripción

African American

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085756
history of hypertension
Descripción

Hypertensive disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020538
patient at a participating site
Descripción

Patient Participation Site

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C2825164
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of chronic kidney disease
Descripción

Chronic Kidney Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1561643
history of diabetes
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
pregnant
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
cognitively impaired/unable to provide consent
Descripción

Impaired cognition | Informed Consent Unable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
terminally ill
Descripción

Terminal illness

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0679247
planning to leave area of study permanently during the one year study period
Descripción

Plan Relocation of home Study Site

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301732
UMLS CUI [1,2]
C2699029
UMLS CUI [1,3]
C2825164

Similar models

Eligibility Hypertension NCT02234063

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
ages18-65
boolean
C0001779 (UMLS CUI [1])
African American
Item
self-identifies as black/african american
boolean
C0085756 (UMLS CUI [1])
Hypertensive disease
Item
history of hypertension
boolean
C0020538 (UMLS CUI [1])
Patient Participation Site
Item
patient at a participating site
boolean
C0030705 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Chronic Kidney Disease
Item
history of chronic kidney disease
boolean
C1561643 (UMLS CUI [1])
Diabetes Mellitus
Item
history of diabetes
boolean
C0011849 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
Impaired cognition | Informed Consent Unable
Item
cognitively impaired/unable to provide consent
boolean
C0338656 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Terminal illness
Item
terminally ill
boolean
C0679247 (UMLS CUI [1])
Plan Relocation of home Study Site
Item
planning to leave area of study permanently during the one year study period
boolean
C1301732 (UMLS CUI [1,1])
C2699029 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])

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