ID

39925

Beschrijving

FOCUS (Nifedipine GITS's Effect on Central Pressure Assessed by Applanation Tonometry); ODM derived from: https://clinicaltrials.gov/show/NCT01071122

Link

https://clinicaltrials.gov/show/NCT01071122

Trefwoorden

Versies (1)
  1. 04-03-20 04-03-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

4 maart 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hypertension NCT01071122

Engels

Eligibility Hypertension NCT01071122

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
untreated grade 2 or grade 3 hypertension defined by mean diastolic blood pressure (bp) >/= 100 and/or mean systolic bp >/= 160mmhg without anti-hypertensive treatment or treated grade 2 hypertension defined by mean diastolic bp >/= 100 and/or mean systolic bp >/=160mmhg with current diuretics and/or beta-blockers use for >/= 4 weeks
Beschrijving

Hypertensive disease Grade Untreated | Diastolic blood pressure mean | Systolic Pressure mean | Antihypertensive therapy Absent | Hypertensive disease Grade Treated | Diuretics | Adrenergic beta-1 Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0441800
UMLS CUI [1,3]
C0332155
UMLS CUI [2,1]
C0428883
UMLS CUI [2,2]
C0444504
UMLS CUI [3,1]
C0871470
UMLS CUI [3,2]
C0444504
UMLS CUI [4,1]
C0585941
UMLS CUI [4,2]
C0332197
UMLS CUI [5,1]
C0020538
UMLS CUI [5,2]
C0441800
UMLS CUI [5,3]
C1522326
UMLS CUI [6]
C0012798
UMLS CUI [7]
C0304516
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary form of hypertension
Beschrijving

Secondary hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
mean systolic bp >/= 200mmhg and or mean diastolic bp >/= 120mmhg
Beschrijving

Systolic Pressure mean | Diastolic blood pressure mean

Datatype

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0444504
UMLS CUI [2,1]
C0428883
UMLS CUI [2,2]
C0444504
treated with other antihypertensive medication except diuretics or beta-blockers
Beschrijving

Antihypertensive Agents Other | Exception Diuretics | Exception Adrenergic beta-1 Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0205394
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0012798
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0304516
type 1 diabetes mellitus
Beschrijving

Diabetes Mellitus, Insulin-Dependent

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
known cardiovascular disease including history of angina pectoris, heart failure, history of myocardial infarction or revascularization procedure, or cerebrovascular disease (including stroke and transient ischaemic attack) within the previous 12 months
Beschrijving

Cardiovascular Disease | Angina Pectoris | Heart failure | Myocardial Infarction | Revascularization | Cerebrovascular Disorders | Cerebrovascular accident | Transient Ischemic Attack

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0002962
UMLS CUI [3]
C0018801
UMLS CUI [4]
C0027051
UMLS CUI [5]
C0581603
UMLS CUI [6]
C0007820
UMLS CUI [7]
C0038454
UMLS CUI [8]
C0007787
renal insufficiency defined as a serum creatinine: >/= 1.7 mg/dl
Beschrijving

Renal Insufficiency | Creatinine measurement, serum

Datatype

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
pregnancy or not using contraceptive in childbearing aged women
Beschrijving

Pregnancy | Childbearing Potential Contraceptive methods Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0332197
breast feeding women
Beschrijving

Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0006147
any disease or condition that in the opinion of the investigator may interfere with completion of the study
Beschrijving

Disease Interferes with Completion of clinical trial | Condition Interferes with Completion of clinical trial

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2732579
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C2732579
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Similar models

Eligibility Hypertension NCT01071122

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Hypertensive disease Grade Untreated | Diastolic blood pressure mean | Systolic Pressure mean | Antihypertensive therapy Absent | Hypertensive disease Grade Treated | Diuretics | Adrenergic beta-1 Receptor Antagonists
Item
untreated grade 2 or grade 3 hypertension defined by mean diastolic blood pressure (bp) >/= 100 and/or mean systolic bp >/= 160mmhg without anti-hypertensive treatment or treated grade 2 hypertension defined by mean diastolic bp >/= 100 and/or mean systolic bp >/=160mmhg with current diuretics and/or beta-blockers use for >/= 4 weeks
boolean
C0020538 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0332155 (UMLS CUI [1,3])
C0428883 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
C0871470 (UMLS CUI [3,1])
C0444504 (UMLS CUI [3,2])
C0585941 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0020538 (UMLS CUI [5,1])
C0441800 (UMLS CUI [5,2])
C1522326 (UMLS CUI [5,3])
C0012798 (UMLS CUI [6])
C0304516 (UMLS CUI [7])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
secondary form of hypertension
boolean
C0155616 (UMLS CUI [1])
Systolic Pressure mean | Diastolic blood pressure mean
Item
mean systolic bp >/= 200mmhg and or mean diastolic bp >/= 120mmhg
boolean
C0871470 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0444504 (UMLS CUI [2,2])
Antihypertensive Agents Other | Exception Diuretics | Exception Adrenergic beta-1 Receptor Antagonists
Item
treated with other antihypertensive medication except diuretics or beta-blockers
boolean
C0003364 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0012798 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0304516 (UMLS CUI [3,2])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
Cardiovascular Disease | Angina Pectoris | Heart failure | Myocardial Infarction | Revascularization | Cerebrovascular Disorders | Cerebrovascular accident | Transient Ischemic Attack
Item
known cardiovascular disease including history of angina pectoris, heart failure, history of myocardial infarction or revascularization procedure, or cerebrovascular disease (including stroke and transient ischaemic attack) within the previous 12 months
boolean
C0007222 (UMLS CUI [1])
C0002962 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0581603 (UMLS CUI [5])
C0007820 (UMLS CUI [6])
C0038454 (UMLS CUI [7])
C0007787 (UMLS CUI [8])
Renal Insufficiency | Creatinine measurement, serum
Item
renal insufficiency defined as a serum creatinine: >/= 1.7 mg/dl
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Pregnancy | Childbearing Potential Contraceptive methods Absent
Item
pregnancy or not using contraceptive in childbearing aged women
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Breast Feeding
Item
breast feeding women
boolean
C0006147 (UMLS CUI [1])
Disease Interferes with Completion of clinical trial | Condition Interferes with Completion of clinical trial
Item
any disease or condition that in the opinion of the investigator may interfere with completion of the study
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C2732579 (UMLS CUI [2,3])
Terug naar het begin van de pagina 

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