Eligibility Kidney, Polycystic, Autosomal Dominant NCT00890279

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
adpkd patients
Descripción

Polycystic Kidney Disease, Autosomal Dominant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085413
blood pressure measured at out-patient setting is above 120/80 mmhg
Descripción

Blood pressure measurement | Outpatient

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005824
UMLS CUI [2]
C0029921
age between 20 and 60 years old
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
egfr more than 30 ml/min/1.73m2
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
patients give informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with severe cardiovascular and hepatic disorders
Descripción

Cardiovascular Disease Severe | Liver disease Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0023895
UMLS CUI [2,2]
C0205082
patients with complications of central nervous vascular disorders
Descripción

Central nervous system vascular disorders Complications

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0851452
UMLS CUI [1,2]
C0009566
women who are breast feeding and females of childbearing potential who are not using acceptable contraceptive methods
Descripción

Breast Feeding | Childbearing Potential Contraceptive methods Absent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0332197
patients currently engaging in other experimental protocol
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
patients with intracranial aneurysma
Descripción

Intracranial Aneurysm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007766
patients who must use diuretics
Descripción

Patient need for Diuretics

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C0012798
allergic patients to candesartan or cilnidipine
Descripción

Hypersensitivity Candesartan | Hypersensitivity Cilnidipine

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0717550
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0378675
patients whose hypertension is not controlled by medication of this protocol
Descripción

Hypertensive disease Control | Pharmaceutical Preparations Study Protocol Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0243148
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C2348563
UMLS CUI [2,3]
C0332197

Similar models

Eligibility Kidney, Polycystic, Autosomal Dominant NCT00890279

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Polycystic Kidney Disease, Autosomal Dominant
Item
adpkd patients
boolean
C0085413 (UMLS CUI [1])
Blood pressure measurement | Outpatient
Item
blood pressure measured at out-patient setting is above 120/80 mmhg
boolean
C0005824 (UMLS CUI [1])
C0029921 (UMLS CUI [2])
Age
Item
age between 20 and 60 years old
boolean
C0001779 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
egfr more than 30 ml/min/1.73m2
boolean
C3811844 (UMLS CUI [1])
Informed Consent
Item
patients give informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cardiovascular Disease Severe | Liver disease Severe
Item
patients with severe cardiovascular and hepatic disorders
boolean
C0007222 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Central nervous system vascular disorders Complications
Item
patients with complications of central nervous vascular disorders
boolean
C0851452 (UMLS CUI [1,1])
C0009566 (UMLS CUI [1,2])
Breast Feeding | Childbearing Potential Contraceptive methods Absent
Item
women who are breast feeding and females of childbearing potential who are not using acceptable contraceptive methods
boolean
C0006147 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Study Subject Participation Status
Item
patients currently engaging in other experimental protocol
boolean
C2348568 (UMLS CUI [1])
Intracranial Aneurysm
Item
patients with intracranial aneurysma
boolean
C0007766 (UMLS CUI [1])
Patient need for Diuretics
Item
patients who must use diuretics
boolean
C0686904 (UMLS CUI [1,1])
C0012798 (UMLS CUI [1,2])
Hypersensitivity Candesartan | Hypersensitivity Cilnidipine
Item
allergic patients to candesartan or cilnidipine
boolean
C0020517 (UMLS CUI [1,1])
C0717550 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0378675 (UMLS CUI [2,2])
Hypertensive disease Control | Pharmaceutical Preparations Study Protocol Absent
Item
patients whose hypertension is not controlled by medication of this protocol
boolean
C0020538 (UMLS CUI [1,1])
C0243148 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])