ID

34339

Beschrijving

Assessment of Aliskiren/Amlodipine and Amlodipine on Ankle Foot Volume (AFV) in Patients With Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01080768

Link

https://clinicaltrials.gov/show/NCT01080768

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hypertension NCT01080768

Eligibility Hypertension NCT01080768

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients (male or female) with hypertension aged between 18-75 yrs.
Beschrijving

ID.1

Datatype

boolean

patients not treated with amlodipine or no amlodipine in previous 1 year.
Beschrijving

ID.2

Datatype

boolean

post-menopausal females
Beschrijving

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients unable to switch from prior hypertensive medication.
Beschrijving

ID.4

Datatype

boolean

severe hypertension.
Beschrijving

ID.5

Datatype

boolean

pregnant or nursing females.
Beschrijving

ID.6

Datatype

boolean

patients with type 1 or type 2 diabetes mellitus
Beschrijving

ID.7

Datatype

boolean

history of immunodeficiency diseases, including a positive human immunodeficiency virus (hiv) (enzyme-linked immunosorbent assay [elisa] and western blot) test result.
Beschrijving

ID.8

Datatype

boolean

a positive hepatitis b surface antigen (hbsag) or hepatitis c test result.
Beschrijving

ID.9

Datatype

boolean

other protocol-defined inclusion/exclusion criteria are applied
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Hypertension NCT01080768

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients (male or female) with hypertension aged between 18-75 yrs.
boolean
ID.2
Item
patients not treated with amlodipine or no amlodipine in previous 1 year.
boolean
ID.3
Item
post-menopausal females
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
patients unable to switch from prior hypertensive medication.
boolean
ID.5
Item
severe hypertension.
boolean
ID.6
Item
pregnant or nursing females.
boolean
ID.7
Item
patients with type 1 or type 2 diabetes mellitus
boolean
ID.8
Item
history of immunodeficiency diseases, including a positive human immunodeficiency virus (hiv) (enzyme-linked immunosorbent assay [elisa] and western blot) test result.
boolean
ID.9
Item
a positive hepatitis b surface antigen (hbsag) or hepatitis c test result.
boolean
ID.10
Item
other protocol-defined inclusion/exclusion criteria are applied
boolean

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