ID

29336

Descrizione

Efficacy and Safety of Once Daily Dosing of Aliskiren (300 mg (qd) Once a Day) to Twice Daily Dosing of Aliskiren (150 mg (Bid) Twice a Day) in Treating Moderate Hypertension.; ODM derived from: https://clinicaltrials.gov/show/NCT00654875

collegamento

https://clinicaltrials.gov/show/NCT00654875

Keywords

versioni (1)
  1. 19/03/18 19/03/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

19 marzo 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Essential Hypertension NCT00654875

Inglese

Eligibility Essential Hypertension NCT00654875

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
have diagnosis of uncomplicated essential hypertension; newly diagnosed or who have not received antihypertension medication within 4 weeks of visit 1 must have an office cuff mean sitting diastolic blood pressure (msdbp) > 100 mmhg and < 110 mmhg at visit 1. if patient is receiving antihypertensive treatment, must have a cuff msdbp > 95 mmhg and < 110 mmhg at visit 1
Descrizione

Essential Hypertension Uncomplicated | Antihypertensive Agents Absent | Sitting diastolic blood pressure mean | Relationship Antihypertensive therapy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0085580
UMLS CUI [1,2]
C0443334
UMLS CUI [2,1]
C0003364
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C1319894
UMLS CUI [3,2]
C0444504
UMLS CUI [4,1]
C0439849
UMLS CUI [4,2]
C0585941
prior to randomization, all patients must have an office cuff msdbp >or= 100 mmhg and <or = 110 mmhg.
Descrizione

Sitting diastolic blood pressure mean

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1319894
UMLS CUI [1,2]
C0444504
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
participation in another aliskiren trial or previous treatment with aliskiren during last 6 months and who qualified to be randomized or enrolled into the active drug treatment period
Descrizione

Study Subject Participation Status | aliskiren

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C1120110
pregnant or nursing women
Descrizione

Pregnancy | Breast Feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
women of child bearing potential unwilling to use protocol specific contraceptive methods
Descrizione

Childbearing Potential Contraceptive methods Unwilling

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0558080
office cuff blood pressure of msdbp ≥ 112 mmhg and/or mean sitting systolic blood pressure (mssbp) ≥ 200 mmhg).
Descrizione

Sitting diastolic blood pressure mean | Sitting systolic blood pressure mean

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1319894
UMLS CUI [1,2]
C0444504
UMLS CUI [2,1]
C1319893
UMLS CUI [2,2]
C0444504
secondary form of hypertension
Descrizione

Secondary hypertension

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0155616
history of heart failure new york heart association (nyha class ii, iii and iv)
Descrizione

Heart failure New York Heart Association Classification

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
previous history of hypertensive encephalopathy or stroke, transient ischemic attack (tia), heart attack, coronary bypass surgery or any percutaneous coronary intervention (pci)
Descrizione

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

Tipo di dati

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
elevated serum potassium (> or = 5.3 meq/l (mmol/l) at visit 1
Descrizione

Serum potassium increased

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0553704
type 1 or type 2 diabetes mellitus not well controlled
Descrizione

Insulin-Dependent Diabetes Mellitus Poorly controlled | Non-Insulin-Dependent Diabetes Mellitus Poorly controlled

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0011854
UMLS CUI [1,2]
C3853134
UMLS CUI [2,1]
C0011860
UMLS CUI [2,2]
C3853134
other protocol-defined inclusion/exclusion criteria may apply
Descrizione

Clinical Trial Eligibility Criteria Study Protocol

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563
Ritorna all'inizio della pagina

Similar models

Eligibility Essential Hypertension NCT00654875

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Essential Hypertension Uncomplicated | Antihypertensive Agents Absent | Sitting diastolic blood pressure mean | Relationship Antihypertensive therapy
Item
have diagnosis of uncomplicated essential hypertension; newly diagnosed or who have not received antihypertension medication within 4 weeks of visit 1 must have an office cuff mean sitting diastolic blood pressure (msdbp) > 100 mmhg and < 110 mmhg at visit 1. if patient is receiving antihypertensive treatment, must have a cuff msdbp > 95 mmhg and < 110 mmhg at visit 1
boolean
C0085580 (UMLS CUI [1,1])
C0443334 (UMLS CUI [1,2])
C0003364 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1319894 (UMLS CUI [3,1])
C0444504 (UMLS CUI [3,2])
C0439849 (UMLS CUI [4,1])
C0585941 (UMLS CUI [4,2])
Sitting diastolic blood pressure mean
Item
prior to randomization, all patients must have an office cuff msdbp >or= 100 mmhg and <or = 110 mmhg.
boolean
C1319894 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status | aliskiren
Item
participation in another aliskiren trial or previous treatment with aliskiren during last 6 months and who qualified to be randomized or enrolled into the active drug treatment period
boolean
C2348568 (UMLS CUI [1])
C1120110 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or nursing women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Unwilling
Item
women of child bearing potential unwilling to use protocol specific contraceptive methods
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
Sitting diastolic blood pressure mean | Sitting systolic blood pressure mean
Item
office cuff blood pressure of msdbp ≥ 112 mmhg and/or mean sitting systolic blood pressure (mssbp) ≥ 200 mmhg).
boolean
C1319894 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
C1319893 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Secondary hypertension
Item
secondary form of hypertension
boolean
C0155616 (UMLS CUI [1])
Heart failure New York Heart Association Classification
Item
history of heart failure new york heart association (nyha class ii, iii and iv)
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Hypertensive Encephalopathy | Cerebrovascular accident | Transient Ischemic Attack | Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
previous history of hypertensive encephalopathy or stroke, transient ischemic attack (tia), heart attack, coronary bypass surgery or any percutaneous coronary intervention (pci)
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])
Serum potassium increased
Item
elevated serum potassium (> or = 5.3 meq/l (mmol/l) at visit 1
boolean
C0553704 (UMLS CUI [1])
Insulin-Dependent Diabetes Mellitus Poorly controlled | Non-Insulin-Dependent Diabetes Mellitus Poorly controlled
Item
type 1 or type 2 diabetes mellitus not well controlled
boolean
C0011854 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0011860 (UMLS CUI [2,1])
C3853134 (UMLS CUI [2,2])
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])
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

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