ID

21063

Descrição

Safety/Efficacy of Combo Therapy With Aliskiren & Hydrochlorothiazide vs Therapy With Hydrochlorothiazide Alone in Patients With Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00387517

Link

https://clinicaltrials.gov/show/NCT00387517

Palavras-chave

Versões (1)
  1. 06/04/2017 06/04/2017 -
Transferido a

6 de abril de 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Hypertension NCT00387517

Inglês

Eligibility Hypertension NCT00387517

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female outpatients 18 years old or older.
Descrição

Outpatients | Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0001779
patients with a diagnosis of hypertension defined as follows:
Descrição

Hypertensive disease

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0020538
newly diagnosed patients or patients who have not been treated for hypertension within the 4 weeks prior to visit 1 must have a msdbp >= mmhg and < 110 mmhg at visit 1.
Descrição

Hypertensive disease Newly Diagnosed | Hypertensive disease Untreated | Sitting diastolic blood pressure mean

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1518321
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C0332155
UMLS CUI [3,1]
C1319894
UMLS CUI [3,2]
C0444504
all patients who have been treated for hypertension within the 4 weeks prior to visit 1 must have a msdbp >= 85 mmhg and < 110 mmhg at visit 2.
Descrição

Hypertensive disease Treated | Sitting diastolic blood pressure mean

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1522326
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
all patients must have a msdbp >= 90 mmhg and < 110 mmhg at visit 5.
Descrição

Patients All | Sitting diastolic blood pressure mean

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0444868
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
patients who are eligible and consent to participate in the study
Descrição

Study Subject Participation Status | Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

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

Hypertension, severe | Sitting diastolic blood pressure mean | Sitting systolic blood pressure mean

Tipo de dados

boolean

Alias
UMLS CUI [1]
C4013784
UMLS CUI [2,1]
C1319894
UMLS CUI [2,2]
C0444504
UMLS CUI [3,1]
C1319893
UMLS CUI [3,2]
C0444504
previous or current diagnosis of heart failure.
Descrição

Heart failure

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0018801
history of hypertensive encephalopathy or cerebrovascular accident, transient ischemic cerebral attack, myocardial infarction, coronary bypass surgery, or any percutaneous coronary intervention.
Descrição

Hypertensive Encephalopathy | Cerebrovascular accident | Transient Ischemic Attack | Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0151620
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0007787
UMLS CUI [4]
C0027051
UMLS CUI [5]
C0010055
UMLS CUI [6]
C1532338
other protocol-defined inclusion/exclusion criteria may apply
Descrição

Clinical Trial Eligibility Criteria Study Protocol

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563
Voltar ao início da página

Similar models

Eligibility Hypertension NCT00387517

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients | Age
Item
male or female outpatients 18 years old or older.
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Hypertensive disease
Item
patients with a diagnosis of hypertension defined as follows:
boolean
C0020538 (UMLS CUI [1])
Hypertensive disease Newly Diagnosed | Hypertensive disease Untreated | Sitting diastolic blood pressure mean
Item
newly diagnosed patients or patients who have not been treated for hypertension within the 4 weeks prior to visit 1 must have a msdbp >= mmhg and < 110 mmhg at visit 1.
boolean
C0020538 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
C1319894 (UMLS CUI [3,1])
C0444504 (UMLS CUI [3,2])
Hypertensive disease Treated | Sitting diastolic blood pressure mean
Item
all patients who have been treated for hypertension within the 4 weeks prior to visit 1 must have a msdbp >= 85 mmhg and < 110 mmhg at visit 2.
boolean
C0020538 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Patients All | Sitting diastolic blood pressure mean
Item
all patients must have a msdbp >= 90 mmhg and < 110 mmhg at visit 5.
boolean
C0030705 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Study Subject Participation Status | Informed Consent
Item
patients who are eligible and consent to participate in the study
boolean
C2348568 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Hypertension, severe | Sitting diastolic blood pressure mean | Sitting systolic blood pressure mean
Item
severe hypertension (msdbp >= 110 mmhg and/or mssbp >=180 mmhg).
boolean
C4013784 (UMLS CUI [1])
C1319894 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
C1319893 (UMLS CUI [3,1])
C0444504 (UMLS CUI [3,2])
Heart failure
Item
previous or current diagnosis of heart failure.
boolean
C0018801 (UMLS CUI [1])
Hypertensive Encephalopathy | Cerebrovascular accident | Transient Ischemic Attack | Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
history of hypertensive encephalopathy or cerebrovascular accident, transient ischemic cerebral attack, myocardial infarction, coronary bypass surgery, or any percutaneous coronary intervention.
boolean
C0151620 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0010055 (UMLS CUI [5])
C1532338 (UMLS CUI [6])
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])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial