ID

34339

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01080768

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hypertension NCT01080768

Eligibility Hypertension NCT01080768

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

post-menopausal females
Beskrivning

ID.3

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.4

Datatyp

boolean

severe hypertension.
Beskrivning

ID.5

Datatyp

boolean

pregnant or nursing females.
Beskrivning

ID.6

Datatyp

boolean

patients with type 1 or type 2 diabetes mellitus
Beskrivning

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

other protocol-defined inclusion/exclusion criteria are applied
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Hypertension NCT01080768

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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