ID

21070

Description

An Assessment of Long Term Safety of the Combination of Aliskiren / Amlodipine in Patients With High Blood Pressure; ODM derived from: https://clinicaltrials.gov/show/NCT00402103

Lien

https://clinicaltrials.gov/show/NCT00402103

Mots-clés

  1. 07/04/2017 07/04/2017 -
Téléchargé le

7 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Hypertension NCT00402103

Eligibility Hypertension NCT00402103

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
outpatients 18 years of age or older
Description

Outpatients | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0001779
male or female patients are eligible
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
for newly diagnosed/untreated patients with essential hypertension defined as msdbp ≥
Description

Essential Hypertension Newly Diagnosed | Essential Hypertension Untreated

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085580
UMLS CUI [1,2]
C1518321
UMLS CUI [2,1]
C0085580
UMLS CUI [2,2]
C0332155
90 and < 110 mmhg at visit 1 and visit 4
Description

Sitting diastolic blood pressure mean

Type de données

boolean

Alias
UMLS CUI [1,1]
C1319894
UMLS CUI [1,2]
C0444504
for previously treated patients with essential hypertension defined as msdbp ≥ 90 and < 110 mmhg after 2 to 4 weeks of washout (visit 4)
Description

Essential Hypertension Treated | Sitting diastolic blood pressure mean

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085580
UMLS CUI [1,2]
C1522326
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe hypertension
Description

Hypertension, severe

Type de données

boolean

Alias
UMLS CUI [1]
C4013784
history or evidence of a secondary form of hypertension
Description

Secondary hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C0155616
history of hypertensive encephalopathy or cerebrovascular accident.
Description

Hypertensive Encephalopathy | Cerebrovascular accident

Type de données

boolean

Alias
UMLS CUI [1]
C0151620
UMLS CUI [2]
C0038454
other protocol-defined inclusion/exclusion criteria may apply
Description

Clinical Trial Eligibility Criteria Study Protocol

Type de données

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563

Similar models

Eligibility Hypertension NCT00402103

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients | Age
Item
outpatients 18 years of age or older
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Gender
Item
male or female patients are eligible
boolean
C0079399 (UMLS CUI [1])
Essential Hypertension Newly Diagnosed | Essential Hypertension Untreated
Item
for newly diagnosed/untreated patients with essential hypertension defined as msdbp ≥
boolean
C0085580 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0085580 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
Sitting diastolic blood pressure mean
Item
90 and < 110 mmhg at visit 1 and visit 4
boolean
C1319894 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
Essential Hypertension Treated | Sitting diastolic blood pressure mean
Item
for previously treated patients with essential hypertension defined as msdbp ≥ 90 and < 110 mmhg after 2 to 4 weeks of washout (visit 4)
boolean
C0085580 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Hypertension, severe
Item
severe hypertension
boolean
C4013784 (UMLS CUI [1])
Secondary hypertension
Item
history or evidence of a secondary form of hypertension
boolean
C0155616 (UMLS CUI [1])
Hypertensive Encephalopathy | Cerebrovascular accident
Item
history of hypertensive encephalopathy or cerebrovascular accident.
boolean
C0151620 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Clinical Trial Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])

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