Informatie:
Fout:
ID
21070
Beschrijving
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
Link
https://clinicaltrials.gov/show/NCT00402103
Trefwoorden
Versies (1)
- 07-04-17 07-04-17 -
Geüploaded op
7 april 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT00402103
Eligibility Hypertension NCT00402103
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00402103
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Outpatients | Age
Item
outpatients 18 years of age or older
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
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])
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])
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])
C1522326 (UMLS CUI [1,2])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
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])
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])
C2348563 (UMLS CUI [1,2])