ID

24418

Beschreibung

Sympathetic Nervous System Modulation in Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00491387

Link

https://clinicaltrials.gov/show/NCT00491387

Stichworte

Versionen (1)
  1. 31.07.17 31.07.17 -
Hochgeladen am

31. Juli 2017

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Hypertension NCT00491387

Englisch

Eligibility Hypertension NCT00491387

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
essential hypertension with blood pressure less than 140/90 on either an ace inhibitor or angiotensin receptor blocker
Beschreibung

Essential Hypertension | Blood pressure | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist

Datentyp

boolean

Alias
UMLS CUI [1]
C0085580
UMLS CUI [2]
C1271104
UMLS CUI [3]
C0003015
UMLS CUI [4]
C0521942
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
known valvular heart disease of more than mild severity
Beschreibung

Heart valve disease Moderate | Heart valve disease Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C0018824
UMLS CUI [2,2]
C0205082
known coronary artery disease defined by an angiographic coronary artery stenosis greater than or equal to 50% luminal diameter narrowing, acute or previous myocardial infarction, or previous coronary revascularization
Beschreibung

Coronary Artery Disease | Coronary Stenosis Angiography | Stenosis Lumen Diameter Percentage | Myocardial Infarction | Coronary revascularisation

Datentyp

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2,1]
C0242231
UMLS CUI [2,2]
C0002978
UMLS CUI [3,1]
C1261287
UMLS CUI [3,2]
C3640173
UMLS CUI [3,3]
C0439165
UMLS CUI [4]
C0027051
UMLS CUI [5]
C0877341
known non-ischemic cardiomyopathy with left ventricular ejection fraction less than 50%
Beschreibung

Non-ischemic cardiomyopathy | Left ventricular ejection fraction

Datentyp

boolean

Alias
UMLS CUI [1]
C0877438
UMLS CUI [2]
C0428772
atrial fibrillation
Beschreibung

Atrial Fibrillation

Datentyp

boolean

Alias
UMLS CUI [1]
C0004238
current treatment with a β-adrenergic blocking drug or a calcium channel blocker
Beschreibung

Adrenergic Antagonists | Calcium Channel Blockers

Datentyp

boolean

Alias
UMLS CUI [1]
C0242889
UMLS CUI [2]
C0006684
current treatment with a psychoactive or other drug known to alter 123i-mibg uptake
Beschreibung

Psychotropic Drugs Changing 123I-mIBG Uptake | Pharmaceutical Preparations Changing 123I-mIBG Uptake

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0033978
UMLS CUI [1,2]
C0392747
UMLS CUI [1,3]
C1276981
UMLS CUI [1,4]
C0243144
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0392747
UMLS CUI [2,3]
C1276981
UMLS CUI [2,4]
C0243144
participation in another research study within the prior 30 days
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
a life-limiting disease process that is likely to preclude completion of study participation
Beschreibung

Disease Limiting Life Expectancy | Study Subject Participation Status Completion Unlikely

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0023671
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C0205197
UMLS CUI [2,3]
C0750558
pregnancy or breast feeding
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
inability or unwillingness to provide informed consent
Beschreibung

Informed Consent Unable | Informed Consent Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
baseline resting heart rate less than 65 beats per minute
Beschreibung

Resting heart rate

Datentyp

boolean

Alias
UMLS CUI [1]
C1821417
diabetes
Beschreibung

Diabetes Mellitus

Datentyp

boolean

Alias
UMLS CUI [1]
C0011849
iodine allergy
Beschreibung

Iodine allergy

Datentyp

boolean

Alias
UMLS CUI [1]
C0571818
unwilling to sign informed consent.
Beschreibung

Informed Consent Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
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Ähnliche Modelle

Eligibility Hypertension NCT00491387

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Essential Hypertension | Blood pressure | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist
Item
essential hypertension with blood pressure less than 140/90 on either an ace inhibitor or angiotensin receptor blocker
boolean
C0085580 (UMLS CUI [1])
C1271104 (UMLS CUI [2])
C0003015 (UMLS CUI [3])
C0521942 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Heart valve disease Moderate | Heart valve disease Severe
Item
known valvular heart disease of more than mild severity
boolean
C0018824 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0018824 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Coronary Artery Disease | Coronary Stenosis Angiography | Stenosis Lumen Diameter Percentage | Myocardial Infarction | Coronary revascularisation
Item
known coronary artery disease defined by an angiographic coronary artery stenosis greater than or equal to 50% luminal diameter narrowing, acute or previous myocardial infarction, or previous coronary revascularization
boolean
C1956346 (UMLS CUI [1])
C0242231 (UMLS CUI [2,1])
C0002978 (UMLS CUI [2,2])
C1261287 (UMLS CUI [3,1])
C3640173 (UMLS CUI [3,2])
C0439165 (UMLS CUI [3,3])
C0027051 (UMLS CUI [4])
C0877341 (UMLS CUI [5])
Non-ischemic cardiomyopathy | Left ventricular ejection fraction
Item
known non-ischemic cardiomyopathy with left ventricular ejection fraction less than 50%
boolean
C0877438 (UMLS CUI [1])
C0428772 (UMLS CUI [2])
Atrial Fibrillation
Item
atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Adrenergic Antagonists | Calcium Channel Blockers
Item
current treatment with a β-adrenergic blocking drug or a calcium channel blocker
boolean
C0242889 (UMLS CUI [1])
C0006684 (UMLS CUI [2])
Psychotropic Drugs Changing 123I-mIBG Uptake | Pharmaceutical Preparations Changing 123I-mIBG Uptake
Item
current treatment with a psychoactive or other drug known to alter 123i-mibg uptake
boolean
C0033978 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C1276981 (UMLS CUI [1,3])
C0243144 (UMLS CUI [1,4])
C0013227 (UMLS CUI [2,1])
C0392747 (UMLS CUI [2,2])
C1276981 (UMLS CUI [2,3])
C0243144 (UMLS CUI [2,4])
Study Subject Participation Status
Item
participation in another research study within the prior 30 days
boolean
C2348568 (UMLS CUI [1])
Disease Limiting Life Expectancy | Study Subject Participation Status Completion Unlikely
Item
a life-limiting disease process that is likely to preclude completion of study participation
boolean
C0012634 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C2348568 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
Pregnancy | Breast Feeding
Item
pregnancy or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Informed Consent Unable | Informed Consent Unwilling
Item
inability or unwillingness to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Resting heart rate
Item
baseline resting heart rate less than 65 beats per minute
boolean
C1821417 (UMLS CUI [1])
Diabetes Mellitus
Item
diabetes
boolean
C0011849 (UMLS CUI [1])
Iodine allergy
Item
iodine allergy
boolean
C0571818 (UMLS CUI [1])
Informed Consent Unwilling
Item
unwilling to sign informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
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