ID

29954

Description

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

Keywords

Versions (1)
  1. 4/29/18 4/29/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

April 29, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Hypertension NCT00770861

English

Eligibility Hypertension NCT00770861

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Outpatients | Age | Hispanics | Latinos

Data type

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
Description

Postmenopausal state | Gender Pregnancy Absent | Gender Contraceptive methods

Data type

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
Description

Hypertensive disease Stage

Data type

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
Description

Therapeutic procedure Absent | Antihypertensive Agents Quantity

Data type

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary hypertension
Description

Secondary hypertension

Data type

boolean

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

Antihypertensive Agents Quantity

Data type

boolean

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

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

Data type

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
Description

Comorbidity Interferes with Clinical Trial | Condition Interferes with Clinical Trial

Data type

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).
Description

Study Subject Participation Status

Data type

boolean

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

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

Data type

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
Back to the top of the page

Similar models

Eligibility Hypertension NCT00770861

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial