ID

34339

Description

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

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Hypertension NCT01080768

Eligibility Hypertension NCT01080768

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

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

ID.2

Data type

boolean

post-menopausal females
Description

ID.3

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.4

Data type

boolean

severe hypertension.
Description

ID.5

Data type

boolean

pregnant or nursing females.
Description

ID.6

Data type

boolean

patients with type 1 or type 2 diabetes mellitus
Description

ID.7

Data type

boolean

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

ID.8

Data type

boolean

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

ID.9

Data type

boolean

other protocol-defined inclusion/exclusion criteria are applied
Description

ID.10

Data type

boolean

Similar models

Eligibility Hypertension NCT01080768

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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