Eligibility Hypertension NCT01355055

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
refractory hypertension (as defined by the who: poorly controlled hypertension (>140/90 mmhg) despite adequate doses of at least three antihypertensive drugs including a diuretic)
Description

Refractory hypertension | Poor hypertension control | Blood pressure determination | Antihypertensive Agents Quantity Dose | Diuretics

Type de données

boolean

Alias
UMLS CUI [1]
C0860493
UMLS CUI [2]
C0421190
UMLS CUI [3]
C0005824
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C1265611
UMLS CUI [4,3]
C0178602
UMLS CUI [5]
C0012798
men or women aged >18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
intact peroneal nerve
Description

Peroneal Nerve Intact

Type de données

boolean

Alias
UMLS CUI [1,1]
C4316912
UMLS CUI [1,2]
C0205266
written informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
diseases, dysfunctions, or medications (such as net inhibitors) that exclude a participation in the study according to the investigator.
Description

Disease Study Subject Participation Status Excluded | Dysfunction Study Subject Participation Status Excluded | Pharmaceutical Preparations Study Subject Participation Status Excluded | Norepinephrine Transporter Inhibitors

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0332196
UMLS CUI [2,1]
C3887504
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C0332196
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C0332196
UMLS CUI [4,1]
C0132800
UMLS CUI [4,2]
C0243077
legal incompetence or circumstances that interfere with the patient´s ability to fully understand scope, relevance, and/or consequences of participation in this study.
Description

Incompetence Legal | Life circumstance problem Interferes with Comprehension Study Protocol

Type de données

boolean

Alias
UMLS CUI [1,1]
C0231189
UMLS CUI [1,2]
C1301860
UMLS CUI [2,1]
C0868647
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C2348563
people in custody
Description

People Guardianship

Type de données

boolean

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C0870627
hypersensitivity to clonidine, phenylephrine, or nitroprusside-sodium
Description

Clonidine allergy | Phenylephrine allergy | Sodium nitroprusside allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0570975
UMLS CUI [2]
C0570949
UMLS CUI [3]
C0571973
sick sinus syndrome, second or third degree av block, bradycardia < 50 bpm (contraindication for clonidine)
Description

Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Bradycardia | Medical contraindication Clonidine

Type de données

boolean

Alias
UMLS CUI [1]
C0037052
UMLS CUI [2]
C0264906
UMLS CUI [3]
C0151517
UMLS CUI [4]
C0428977
UMLS CUI [5,1]
C1301624
UMLS CUI [5,2]
C0009014
endogenous depression (contraindication for clonidine)
Description

Endogenous depression | Medical contraindication Clonidine

Type de données

boolean

Alias
UMLS CUI [1]
C0011573
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0009014

Similar models

Eligibility Hypertension NCT01355055

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Refractory hypertension | Poor hypertension control | Blood pressure determination | Antihypertensive Agents Quantity Dose | Diuretics
Item
refractory hypertension (as defined by the who: poorly controlled hypertension (>140/90 mmhg) despite adequate doses of at least three antihypertensive drugs including a diuretic)
boolean
C0860493 (UMLS CUI [1])
C0421190 (UMLS CUI [2])
C0005824 (UMLS CUI [3])
C0003364 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0178602 (UMLS CUI [4,3])
C0012798 (UMLS CUI [5])
Age
Item
men or women aged >18 years
boolean
C0001779 (UMLS CUI [1])
Peroneal Nerve Intact
Item
intact peroneal nerve
boolean
C4316912 (UMLS CUI [1,1])
C0205266 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Disease Study Subject Participation Status Excluded | Dysfunction Study Subject Participation Status Excluded | Pharmaceutical Preparations Study Subject Participation Status Excluded | Norepinephrine Transporter Inhibitors
Item
diseases, dysfunctions, or medications (such as net inhibitors) that exclude a participation in the study according to the investigator.
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C3887504 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C0132800 (UMLS CUI [4,1])
C0243077 (UMLS CUI [4,2])
Incompetence Legal | Life circumstance problem Interferes with Comprehension Study Protocol
Item
legal incompetence or circumstances that interfere with the patient´s ability to fully understand scope, relevance, and/or consequences of participation in this study.
boolean
C0231189 (UMLS CUI [1,1])
C1301860 (UMLS CUI [1,2])
C0868647 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
People Guardianship
Item
people in custody
boolean
C0027361 (UMLS CUI [1,1])
C0870627 (UMLS CUI [1,2])
Clonidine allergy | Phenylephrine allergy | Sodium nitroprusside allergy
Item
hypersensitivity to clonidine, phenylephrine, or nitroprusside-sodium
boolean
C0570975 (UMLS CUI [1])
C0570949 (UMLS CUI [2])
C0571973 (UMLS CUI [3])
Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Bradycardia | Medical contraindication Clonidine
Item
sick sinus syndrome, second or third degree av block, bradycardia < 50 bpm (contraindication for clonidine)
boolean
C0037052 (UMLS CUI [1])
C0264906 (UMLS CUI [2])
C0151517 (UMLS CUI [3])
C0428977 (UMLS CUI [4])
C1301624 (UMLS CUI [5,1])
C0009014 (UMLS CUI [5,2])
Endogenous depression | Medical contraindication Clonidine
Item
endogenous depression (contraindication for clonidine)
boolean
C0011573 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0009014 (UMLS CUI [2,2])