ID

29954

Descripción

A Study on the Efficacy and Safety of Nebivolol Monotherapy in Hispanic Hypertensive Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00770861

Link

https://clinicaltrials.gov/show/NCT00770861

Palabras clave

Versiones (1)
  1. 29/4/18 29/4/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29 de abril de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Hypertension NCT00770861

Inglés

Eligibility Hypertension NCT00770861

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female outpatients 18 to 80 years of age, self-identified as hispanic or latino ethnicity
Descripción

Outpatients | Age | Hispanics | Latinos

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0086409
UMLS CUI [4]
C0086528
females must be post-menopausal, or not pregnant and using an approved contraceptive regimen
Descripción

Postmenopausal state | Gender Pregnancy Absent | Gender Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2,1]
C0079399
UMLS CUI [2,2]
C0032961
UMLS CUI [2,3]
C0332197
UMLS CUI [3,1]
C0079399
UMLS CUI [3,2]
C0700589
meet criteria for stage i or ii hypertension
Descripción

Hypertensive disease Stage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0699749
currently not treated, or being treated with no more than two anti-hypertensive medications
Descripción

Therapeutic procedure Absent | Antihypertensive Agents Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0003364
UMLS CUI [2,2]
C1265611
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary hypertension
Descripción

Secondary hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155616
are taking three or more antihypertensive agents
Descripción

Antihypertensive Agents Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C1265611
have uncontrolled or poorly controlled diabetes mellitus type i or type ii
Descripción

DIABETES MELLITUS INSULIN DEPENDENT UNCONTROLLED | DIABETES MELLITUS NON INSULIN DEPENDENT UNCONTROLLED | Insulin-Dependent Diabetes Mellitus Poorly controlled | Non-Insulin-Dependent Diabetes Mellitus Poorly controlled

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0743113
UMLS CUI [2]
C0743118
UMLS CUI [3,1]
C0011854
UMLS CUI [3,2]
C3853134
UMLS CUI [4,1]
C0011860
UMLS CUI [4,2]
C3853134
evidence of other concurrent disease or conditions that might interfere with the conduct of the study
Descripción

Comorbidity Interferes with Clinical Trial | Condition Interferes with Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0008976
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0008976
participation in any investigational study within 30 days of screening (visit 1).
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
have a history of hypersensitivity to nebivolol or other β-blockers, or any contraindication to β-blocker use
Descripción

Hypersensitivity Nebivolol | BETA BLOCKER ALLERGY | Medical contraindication Adrenergic beta-1 Receptor Antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0068475
UMLS CUI [2]
C0741466
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C0304516
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Similar models

Eligibility Hypertension NCT00770861

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients | Age | Hispanics | Latinos
Item
male and female outpatients 18 to 80 years of age, self-identified as hispanic or latino ethnicity
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0086409 (UMLS CUI [3])
C0086528 (UMLS CUI [4])
Postmenopausal state | Gender Pregnancy Absent | Gender Contraceptive methods
Item
females must be post-menopausal, or not pregnant and using an approved contraceptive regimen
boolean
C0232970 (UMLS CUI [1])
C0079399 (UMLS CUI [2,1])
C0032961 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
Hypertensive disease Stage
Item
meet criteria for stage i or ii hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0699749 (UMLS CUI [1,2])
Therapeutic procedure Absent | Antihypertensive Agents Quantity
Item
currently not treated, or being treated with no more than two anti-hypertensive medications
boolean
C0087111 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0003364 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Antihypertensive Agents Quantity
Item
are taking three or more antihypertensive agents
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
DIABETES MELLITUS INSULIN DEPENDENT UNCONTROLLED | DIABETES MELLITUS NON INSULIN DEPENDENT UNCONTROLLED | Insulin-Dependent Diabetes Mellitus Poorly controlled | Non-Insulin-Dependent Diabetes Mellitus Poorly controlled
Item
have uncontrolled or poorly controlled diabetes mellitus type i or type ii
boolean
C0743113 (UMLS CUI [1])
C0743118 (UMLS CUI [2])
C0011854 (UMLS CUI [3,1])
C3853134 (UMLS CUI [3,2])
C0011860 (UMLS CUI [4,1])
C3853134 (UMLS CUI [4,2])
Comorbidity Interferes with Clinical Trial | Condition Interferes with Clinical Trial
Item
evidence of other concurrent disease or conditions that might interfere with the conduct of the study
boolean
C0009488 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Study Subject Participation Status
Item
participation in any investigational study within 30 days of screening (visit 1).
boolean
C2348568 (UMLS CUI [1])
Hypersensitivity Nebivolol | BETA BLOCKER ALLERGY | Medical contraindication Adrenergic beta-1 Receptor Antagonists
Item
have a history of hypersensitivity to nebivolol or other β-blockers, or any contraindication to β-blocker use
boolean
C0020517 (UMLS CUI [1,1])
C0068475 (UMLS CUI [1,2])
C0741466 (UMLS CUI [2])
C1301624 (UMLS CUI [3,1])
C0304516 (UMLS CUI [3,2])
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