ID

39918

Descripción

Nebivolol in Patients With Systolic Stage 2 Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01057251

Link

https://clinicaltrials.gov/show/NCT01057251

Palabras clave

Versiones (1)
  1. 4/3/20 4/3/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 de marzo de 2020

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Hypertension NCT01057251

Inglés

Eligibility Hypertension NCT01057251

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male of female, 18 to 64 years of age at screening
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
mean seated heart rate at least 60 bpm
Descripción

Heart rate while sitting mean

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2029904
UMLS CUI [1,2]
C0444504
diagnosed systolic stage 2 hypertension
Descripción

Systolic hypertension Stage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221155
UMLS CUI [1,2]
C0699749
unremarkable physical exam findings
Descripción

Findings Normal Physical Examination

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0205307
UMLS CUI [1,3]
C0031809
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
high risk due to secondary hypertension or former stage 3 hypertension by jnc6
Descripción

High risk | Secondary hypertension | Hypertensive disease Previous Stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4319571
UMLS CUI [2]
C0155616
UMLS CUI [3,1]
C0020538
UMLS CUI [3,2]
C0205156
UMLS CUI [3,3]
C0699749
concurrent conditions (reno, cardiovascular, obesity, thyroid, etc)
Descripción

Comorbidity | Kidney Diseases | Cardiovascular Diseases | Obesity | Thyroid Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0022658
UMLS CUI [3]
C0007222
UMLS CUI [4]
C0028754
UMLS CUI [5]
C0040128
currently taking medication that cannot be stopped during the course of the study
Descripción

Pharmaceutical Preparation Discontinue Unsuccessful

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C1272705
participating other clinical trials
Descripción

Study Subject Participation Status | Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
member of the study center personnel
Descripción

Member Research Personnel

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0680022
UMLS CUI [1,2]
C0035173
documented drug abuse
Descripción

Drug abuse

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013146
contra indication to beta blocker
Descripción

Medical contraindication Adrenergic beta-1 Receptor Antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0304516
abnormal lab finding
Descripción

Laboratory test result abnormal

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0438215
poor compliance
Descripción

Poor compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032646
other conditions judged by investigator that is not suitable for the study
Descripción

Condition Inappropriate Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C0008976
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Similar models

Eligibility Hypertension NCT01057251

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male of female, 18 to 64 years of age at screening
boolean
C0001779 (UMLS CUI [1])
Heart rate while sitting mean
Item
mean seated heart rate at least 60 bpm
boolean
C2029904 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
Systolic hypertension Stage
Item
diagnosed systolic stage 2 hypertension
boolean
C0221155 (UMLS CUI [1,1])
C0699749 (UMLS CUI [1,2])
Findings Normal Physical Examination
Item
unremarkable physical exam findings
boolean
C0037088 (UMLS CUI [1,1])
C0205307 (UMLS CUI [1,2])
C0031809 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
High risk | Secondary hypertension | Hypertensive disease Previous Stage
Item
high risk due to secondary hypertension or former stage 3 hypertension by jnc6
boolean
C4319571 (UMLS CUI [1])
C0155616 (UMLS CUI [2])
C0020538 (UMLS CUI [3,1])
C0205156 (UMLS CUI [3,2])
C0699749 (UMLS CUI [3,3])
Comorbidity | Kidney Diseases | Cardiovascular Diseases | Obesity | Thyroid Diseases
Item
concurrent conditions (reno, cardiovascular, obesity, thyroid, etc)
boolean
C0009488 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0028754 (UMLS CUI [4])
C0040128 (UMLS CUI [5])
Pharmaceutical Preparation Discontinue Unsuccessful
Item
currently taking medication that cannot be stopped during the course of the study
boolean
C0013227 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Trial
Item
participating other clinical trials
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Member Research Personnel
Item
member of the study center personnel
boolean
C0680022 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
Drug abuse
Item
documented drug abuse
boolean
C0013146 (UMLS CUI [1])
Medical contraindication Adrenergic beta-1 Receptor Antagonists
Item
contra indication to beta blocker
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
Laboratory test result abnormal
Item
abnormal lab finding
boolean
C0438215 (UMLS CUI [1])
Poor compliance
Item
poor compliance
boolean
C0032646 (UMLS CUI [1])
Condition Inappropriate Clinical Trial
Item
other conditions judged by investigator that is not suitable for the study
boolean
C0348080 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
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