ID

39974

Description

A Randomized Controlled Study to Assess the Effects of Bisoprolol and Atenolol on Resting Heart Rate and Sympathetic Nervous System's Activity in Subjects With Essential Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01251146

Link

https://clinicaltrials.gov/show/NCT01251146

Keywords

Versions (1)
  1. 3/7/20 3/7/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 7, 2020

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 NCT01251146

English

Eligibility Hypertension NCT01251146

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects aged between 25-65 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
subjects with essential hypertension (eh)
Description

Essential Hypertension

Data type

boolean

Alias
UMLS CUI [1]
C0085580
subjects with systolic blood pressure (sbp) 140-160 millimeter of mercury (mmhg) and diastolic blood pressure (dbp) 90-100 mmhg
Description

Systolic Pressure | Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
subjects with normal sinus rhythm
Description

Normal sinus rhythm

Data type

boolean

Alias
UMLS CUI [1]
C0232202
subjects with resting heart rate (rhr) greater than 70 bpm
Description

RESTING HEART RATE

Data type

boolean

Alias
UMLS CUI [1]
C1821417
subjects who give written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with atrial fibrillation (af)/sick sinus syndrome (sss)/atrioventricular block ii-iii grade (avb ii-iii) without pacemaker
Description

Atrial Fibrillation | Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Pacemaker Absent

Data type

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0037052
UMLS CUI [3]
C0264906
UMLS CUI [4]
C0151517
UMLS CUI [5,1]
C0810633
UMLS CUI [5,2]
C0332197
subjects with bradyarrhythmia/hypotension
Description

Bradyarrhythmia | Hypotension

Data type

boolean

Alias
UMLS CUI [1]
C0079035
UMLS CUI [2]
C0020649
subjects with unstable angina pectoris (uap)/acute myocardial infarction (ami)/heart failure (hf) (new york heart association [nyha] class iii - iv)
Description

Angina, Unstable | Acute myocardial infarction | Heart failure New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0155626
UMLS CUI [3,1]
C0018801
UMLS CUI [3,2]
C1275491
subjects with uncontrolled diabetes mellitus (dm)
Description

Diabetic - poor control

Data type

boolean

Alias
UMLS CUI [1]
C0421258
subjects with bronchial asthma
Description

Asthma

Data type

boolean

Alias
UMLS CUI [1]
C0004096
subjects with gastro-intestinal ulcer or skin ulcer
Description

Gastrointestinal ulcer | Skin Ulcer

Data type

boolean

Alias
UMLS CUI [1]
C0237938
UMLS CUI [2]
C0037299
subjects with liver dysfunction/renal impairment
Description

Liver Dysfunction | Renal Insufficiency

Data type

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C1565489
subjects treated with calcium channel blockers (except amlodipine) or other beta-blockers.
Description

Calcium Channel Blockers | Exception Amlodipine | Adrenergic beta-1 Receptor Antagonists

Data type

boolean

Alias
UMLS CUI [1]
C0006684
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0051696
UMLS CUI [3]
C0304516
subjects with glaucoma
Description

Glaucoma

Data type

boolean

Alias
UMLS CUI [1]
C0017601
subjects with known allergic/intolerance to beta-blocker
Description

BETA BLOCKER ALLERGY | Intolerance to Adrenergic beta-1 Receptor Antagonists

Data type

boolean

Alias
UMLS CUI [1]
C0741466
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0304516
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
subjects who had participated in another clinical study within the last 3 months
Description

Study Subject Participation Status | Clinical Trial

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
subjects who have legal incapacity or limited legal capacity
Description

Legal capacity Lacking | Legal capacity Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C0683673
UMLS CUI [1,2]
C0332268
UMLS CUI [2,1]
C0683673
UMLS CUI [2,2]
C0439801
Back to the top of the page

Similar models

Eligibility Hypertension NCT01251146

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
subjects aged between 25-65 years
boolean
C0001779 (UMLS CUI [1])
Essential Hypertension
Item
subjects with essential hypertension (eh)
boolean
C0085580 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure
Item
subjects with systolic blood pressure (sbp) 140-160 millimeter of mercury (mmhg) and diastolic blood pressure (dbp) 90-100 mmhg
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Normal sinus rhythm
Item
subjects with normal sinus rhythm
boolean
C0232202 (UMLS CUI [1])
RESTING HEART RATE
Item
subjects with resting heart rate (rhr) greater than 70 bpm
boolean
C1821417 (UMLS CUI [1])
Informed Consent
Item
subjects who give written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation | Sick Sinus Syndrome | Second degree atrioventricular block | Complete atrioventricular block | Pacemaker Absent
Item
subjects with atrial fibrillation (af)/sick sinus syndrome (sss)/atrioventricular block ii-iii grade (avb ii-iii) without pacemaker
boolean
C0004238 (UMLS CUI [1])
C0037052 (UMLS CUI [2])
C0264906 (UMLS CUI [3])
C0151517 (UMLS CUI [4])
C0810633 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
Bradyarrhythmia | Hypotension
Item
subjects with bradyarrhythmia/hypotension
boolean
C0079035 (UMLS CUI [1])
C0020649 (UMLS CUI [2])
Angina, Unstable | Acute myocardial infarction | Heart failure New York Heart Association Classification
Item
subjects with unstable angina pectoris (uap)/acute myocardial infarction (ami)/heart failure (hf) (new york heart association [nyha] class iii - iv)
boolean
C0002965 (UMLS CUI [1])
C0155626 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C1275491 (UMLS CUI [3,2])
Diabetic - poor control
Item
subjects with uncontrolled diabetes mellitus (dm)
boolean
C0421258 (UMLS CUI [1])
Asthma
Item
subjects with bronchial asthma
boolean
C0004096 (UMLS CUI [1])
Gastrointestinal ulcer | Skin Ulcer
Item
subjects with gastro-intestinal ulcer or skin ulcer
boolean
C0237938 (UMLS CUI [1])
C0037299 (UMLS CUI [2])
Liver Dysfunction | Renal Insufficiency
Item
subjects with liver dysfunction/renal impairment
boolean
C0086565 (UMLS CUI [1])
C1565489 (UMLS CUI [2])
Calcium Channel Blockers | Exception Amlodipine | Adrenergic beta-1 Receptor Antagonists
Item
subjects treated with calcium channel blockers (except amlodipine) or other beta-blockers.
boolean
C0006684 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0051696 (UMLS CUI [2,2])
C0304516 (UMLS CUI [3])
Glaucoma
Item
subjects with glaucoma
boolean
C0017601 (UMLS CUI [1])
BETA BLOCKER ALLERGY | Intolerance to Adrenergic beta-1 Receptor Antagonists
Item
subjects with known allergic/intolerance to beta-blocker
boolean
C0741466 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0304516 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status | Clinical Trial
Item
subjects who had participated in another clinical study within the last 3 months
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Legal capacity Lacking | Legal capacity Limited
Item
subjects who have legal incapacity or limited legal capacity
boolean
C0683673 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0683673 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
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