ID

12008

Beschrijving

Monotherapy-Controlled Study of Nifedipine Gastrointestinal Therapeutic System and Candesartan Cilexetil in Combination in Subjects With Essential Hypertension Inadequately Controlled on Candesartan Cilexetil; ODM derived from: https://clinicaltrials.gov/show/NCT02047019

Link

https://clinicaltrials.gov/show/NCT02047019

Trefwoorden

Versies (1)
  1. 01-09-15 01-09-15 -
Houder van rechten

ODM derived from: https://clinicaltrials.gov/show/NCT02047019

Geüploaded op

1 september 2015

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Hypertension NCT02047019

Engels

Eligibility Hypertension NCT02047019

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

male and female subjects 18 years or older are eligible.
Beschrijving

aged 18 years or older; female

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0682069
at visit 0, subjects not treated with antihypertensive medications are to have mssbp (mean seated systolic blood pressure) of >/= 160 mmhg and < 200 mmhg, and 24 hours masbp (mean ambulatory systolic blood pressure) >/= 130 mmhg; those subjects treated with antihypertensive medication are to have mssbp >/= 150 mmhg and < 200 mmhg as measured by a calibrated electronic bp measuring device
Beschrijving

blood pressure; medications; not treated; ambulatory; systolic; device; visit

Datatype

boolean

Alias
UMLS CUI [1]
C0277883
at visit 3,subject must have mssbp >/= 140 mmhg before randomization
Beschrijving

randomization; visit

Datatype

boolean

Alias
UMLS CUI [1]
C0277883
women of childbearing potential and men must agree to use adequate contraception other than hormonal contraceptives when sexually active. this applies since signing of the ic (informed consent)form until the last study drug administration.
Beschrijving

adequate contraception; childbearing potential; informed consent; contraceptives; hormonal; other; active; agree; study; last; drug

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Beschrijving

Exclusion Criteria

mean seated systolic blood pressure (mssbp) >/= 200 mmhg and/or mean seated diastolic blood pressure (msdbp) >/= 120 mm/hg
Beschrijving

diastolic blood pressure; systolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0428883
UMLS CUI [2]
C0871470
mean seated diastolic blood pressure (msdbp) < 60 mm/hg
Beschrijving

diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0428883
differences greater than 20 mmhg for systolic blood pressure (sbp) and 10 mmhg for diastolic blood pressure (dbp) are present on 3 consecutive blood pressure readings at visit 0
Beschrijving

systolic blood pressure (sbp); diastolic blood pressure; present; visit; dbp

Datatype

boolean

Alias
UMLS CUI [1]
C3160850
evidence of secondary hypertension such as coarctation of the aorta, pheochromocytoma, hyperaldosteronism, etc.
Beschrijving

hypertension; evidence of; aorta

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
cerebrovascular ischemic event (stroke, transient ischemic attack [tia]) within the previous 12 months
Beschrijving

transient ischemic attack; stroke; event

Datatype

boolean

Alias
UMLS CUI [1]
C1561291
history of hypertensive retinopathy - known keith-wagener grade iii or iv. any history of heart failure, new york heart association (nyha) classification iii or iv
Beschrijving

new york heart association classification; heart failure; retinopathy; grade; iii

Datatype

boolean

Alias
UMLS CUI [1]
C0152132
UMLS CUI [2]
C0018802
severe coronary heart disease as manifest by a history of myocardial infarction or unstable angina in the last 6 months prior to visit 0
Beschrijving

past history of myocardial infarction; coronary heart disease; unstable angina; severe; visit; last

Datatype

boolean

Alias
UMLS CUI [1]
C0010068
clinically significant cardiac valvular disease
Beschrijving

clinically significant; disease; cardiac

Datatype

boolean

Alias
UMLS CUI [1]
C0018824
subjects with an aortic aneurysm that, in the opinion of the investigator, will be unsuitable to be enrolled in the study.
Beschrijving

aortic aneurysm; investigator; study

Datatype

boolean

Alias
UMLS CUI [1]
C0003486
type 1 diabetes mellitus (dm) or poorly controlled type 2 dm as evidenced by glycosylated hemoglobin hba1c of greater than 9% on visit 0
Beschrijving

type 1 diabetes mellitus; hemoglobin; controlled; visit; hba1c

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
Terug naar het begin van de pagina

Similar models

Eligibility Hypertension NCT02047019

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
aged 18 years or older; female
Item
male and female subjects 18 years or older are eligible.
boolean
C0001779 (UMLS CUI [1])
C0682069 (UMLS CUI [2])
blood pressure; medications; not treated; ambulatory; systolic; device; visit
Item
at visit 0, subjects not treated with antihypertensive medications are to have mssbp (mean seated systolic blood pressure) of >/= 160 mmhg and < 200 mmhg, and 24 hours masbp (mean ambulatory systolic blood pressure) >/= 130 mmhg; those subjects treated with antihypertensive medication are to have mssbp >/= 150 mmhg and < 200 mmhg as measured by a calibrated electronic bp measuring device
boolean
C0277883 (UMLS CUI [1])
randomization; visit
Item
at visit 3,subject must have mssbp >/= 140 mmhg before randomization
boolean
C0277883 (UMLS CUI [1])
adequate contraception; childbearing potential; informed consent; contraceptives; hormonal; other; active; agree; study; last; drug
Item
women of childbearing potential and men must agree to use adequate contraception other than hormonal contraceptives when sexually active. this applies since signing of the ic (informed consent)form until the last study drug administration.
boolean
C0700589 (UMLS CUI [1])
diastolic blood pressure; systolic blood pressure
Item
mean seated systolic blood pressure (mssbp) >/= 200 mmhg and/or mean seated diastolic blood pressure (msdbp) >/= 120 mm/hg
boolean
C0428883 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
diastolic blood pressure
Item
mean seated diastolic blood pressure (msdbp) < 60 mm/hg
boolean
C0428883 (UMLS CUI [1])
systolic blood pressure (sbp); diastolic blood pressure; present; visit; dbp
Item
differences greater than 20 mmhg for systolic blood pressure (sbp) and 10 mmhg for diastolic blood pressure (dbp) are present on 3 consecutive blood pressure readings at visit 0
boolean
C3160850 (UMLS CUI [1])
hypertension; evidence of; aorta
Item
evidence of secondary hypertension such as coarctation of the aorta, pheochromocytoma, hyperaldosteronism, etc.
boolean
C0155616 (UMLS CUI [1])
transient ischemic attack; stroke; event
Item
cerebrovascular ischemic event (stroke, transient ischemic attack [tia]) within the previous 12 months
boolean
C1561291 (UMLS CUI [1])
new york heart association classification; heart failure; retinopathy; grade; iii
Item
history of hypertensive retinopathy - known keith-wagener grade iii or iv. any history of heart failure, new york heart association (nyha) classification iii or iv
boolean
C0152132 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
past history of myocardial infarction; coronary heart disease; unstable angina; severe; visit; last
Item
severe coronary heart disease as manifest by a history of myocardial infarction or unstable angina in the last 6 months prior to visit 0
boolean
C0010068 (UMLS CUI [1])
clinically significant; disease; cardiac
Item
clinically significant cardiac valvular disease
boolean
C0018824 (UMLS CUI [1])
aortic aneurysm; investigator; study
Item
subjects with an aortic aneurysm that, in the opinion of the investigator, will be unsuitable to be enrolled in the study.
boolean
C0003486 (UMLS CUI [1])
type 1 diabetes mellitus; hemoglobin; controlled; visit; hba1c
Item
type 1 diabetes mellitus (dm) or poorly controlled type 2 dm as evidenced by glycosylated hemoglobin hba1c of greater than 9% on visit 0
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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