ID

23207

Descrição

Safety and Efficacy of Aliskiren 300 mg, 150 mg and 75 mg in Patients With Essential Hypertension Compared to Ramipril 5 mg; ODM derived from: https://clinicaltrials.gov/show/NCT00529451

Link

https://clinicaltrials.gov/show/NCT00529451

Palavras-chave

  1. 28/06/2017 28/06/2017 -
Transferido a

28 de junho de 2017

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Hypertension NCT00529451

Eligibility Hypertension NCT00529451

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have msdbp ≥ 90 mmhg and < 110 mmhg at the visit immediately prior to visit 3
Descrição

ID.1

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0005823
patients must have msdbp >or= 95 mmhg and < 110 mmhg at visit 3
Descrição

ID.2

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0005823
patients must have an absolute difference of < or =10 mmhg in their mean sitting diastolic blood pressure (msdbp) from visit 2 to visit 3
Descrição

ID.3

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C1705241
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe hypertension (grade 3 who classification; msdbp >or= 110 mmhg and/or mssbp >or = 180 mmhg).
Descrição

ID.4

Tipo de dados

boolean

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

ID.5

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0155616
history of transient ischemic cerebral attack within 12 months of visit 1.
Descrição

ID.6

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0007787
current angina pectoris requiring pharmacological therapy (other than those patients on a stable dose of oral or topical nitrates)
Descrição

ID.7

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0002962
type 1 or type 2 diabetes mellitus with glycosylated hemoglobin (hba1c) > 8% at visit 1.
Descrição

ID.8

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0011849
known or suspected contraindications to the study medications, including history of allergy to ramipril or other ace inhibitors.
Descrição

ID.9

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0683526
UMLS CUI [1,2]
C0571943
UMLS CUI [1,3]
C0571939
other protocol-defined inclusion/exclusion criteria may apply.
Descrição

ID.10

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251

Similar models

Eligibility Hypertension NCT00529451

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients must have msdbp ≥ 90 mmhg and < 110 mmhg at the visit immediately prior to visit 3
boolean
C0005823 (UMLS CUI [1])
ID.2
Item
patients must have msdbp >or= 95 mmhg and < 110 mmhg at visit 3
boolean
C0005823 (UMLS CUI [1])
ID.3
Item
patients must have an absolute difference of < or =10 mmhg in their mean sitting diastolic blood pressure (msdbp) from visit 2 to visit 3
boolean
C0005823 (UMLS CUI [1,1])
C1705241 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ID.4
Item
severe hypertension (grade 3 who classification; msdbp >or= 110 mmhg and/or mssbp >or = 180 mmhg).
boolean
C4013784 (UMLS CUI [1])
ID.5
Item
history or evidence of a secondary form of hypertension.
boolean
C0155616 (UMLS CUI [1])
ID.6
Item
history of transient ischemic cerebral attack within 12 months of visit 1.
boolean
C0007787 (UMLS CUI [1])
ID.7
Item
current angina pectoris requiring pharmacological therapy (other than those patients on a stable dose of oral or topical nitrates)
boolean
C0002962 (UMLS CUI [1])
ID.8
Item
type 1 or type 2 diabetes mellitus with glycosylated hemoglobin (hba1c) > 8% at visit 1.
boolean
C0011849 (UMLS CUI [1])
ID.9
Item
known or suspected contraindications to the study medications, including history of allergy to ramipril or other ace inhibitors.
boolean
C0683526 (UMLS CUI [1,1])
C0571943 (UMLS CUI [1,2])
C0571939 (UMLS CUI [1,3])
ID.10
Item
other protocol-defined inclusion/exclusion criteria may apply.
boolean
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])

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