ID

31522

Description

Efficacy of Coreg CR and Lisinopril on Markers for Cardiovascular Functional and Structural Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00553969

Lien

https://clinicaltrials.gov/show/NCT00553969

Mots-clés

  1. 31/08/2018 31/08/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

31 août 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Pre-hypertension NCT00553969

Eligibility Pre-hypertension NCT00553969

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females > 18 years old with pre-hypertensive or borderline blood pressures (systolic blood pressure ≥ 130 mmhg or diastolic blood pressure ≥ 85 mmhg) deemed not to need antihypertensive therapy. subjects must also have one additional risk factor for cardiovascular disease, including:
Description

Age | Prehypertension | Borderline blood pressure | Systolic Pressure | Diastolic blood pressure | Antihypertensive therapy Redundant | Risk factor Additional Cardiovascular Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C1696708
UMLS CUI [3]
C1278395
UMLS CUI [4]
C0871470
UMLS CUI [5]
C0428883
UMLS CUI [6,1]
C0585941
UMLS CUI [6,2]
C1313915
UMLS CUI [7,1]
C0035648
UMLS CUI [7,2]
C1524062
UMLS CUI [7,3]
C0007222
ldl > 130 and < 160 mg/dl
Description

Low density lipoprotein cholesterol measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0202117
hdl < 40 mg/dl
Description

High density lipoprotein measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0392885
fasting blood sugar >100 and < 126 mg/dl
Description

Fasting Blood Sugar Measurement

Type de données

boolean

Alias
UMLS CUI [1]
C2825162
body mass index ≥ 30
Description

Body mass index

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
smoker
Description

Tobacco use

Type de données

boolean

Alias
UMLS CUI [1]
C0543414
family history of premature heart disease or hypertension
Description

Family history Premature Heart disease | FH: Hypertension

Type de données

boolean

Alias
UMLS CUI [1,1]
C0241889
UMLS CUI [1,2]
C2749803
UMLS CUI [2]
C0455405
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of cardiac, cerebral or other vascular events within the previous 6 months will be excluded. other exclusions include background therapy with a beta blocker or ace inhibitor therapy, known or suspected intolerance to beta blockers or ace inhibitors, angiotensin receptor blocker therapy, or diabetes. pregnant or lactating women, and women of child-bearing age who are not using an acceptable form of contraception are also excluded from this study.
Description

Cardiac event | Cerebral disorder | Vascular Diseases | Adrenergic beta-Antagonists | ACE Inhibitors | Intolerance to Adrenergic beta-Antagonists | Intolerance to ACE Inhibitors | Intolerance Suspected Adrenergic beta-Antagonists | Intolerance Suspected ACE Inhibitors | Angiotensin II receptor antagonist | Diabetes Mellitus | Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent

Type de données

boolean

Alias
UMLS CUI [1]
C0741923
UMLS CUI [2]
C0234387
UMLS CUI [3]
C0042373
UMLS CUI [4]
C0001645
UMLS CUI [5]
C0003015
UMLS CUI [6,1]
C1744706
UMLS CUI [6,2]
C0001645
UMLS CUI [7,1]
C1744706
UMLS CUI [7,2]
C0003015
UMLS CUI [8,1]
C1744706
UMLS CUI [8,2]
C0750491
UMLS CUI [8,3]
C0001645
UMLS CUI [9,1]
C1744706
UMLS CUI [9,2]
C0750491
UMLS CUI [9,3]
C0003015
UMLS CUI [10]
C0521942
UMLS CUI [11]
C0011849
UMLS CUI [12]
C0032961
UMLS CUI [13]
C0006147
UMLS CUI [14,1]
C3831118
UMLS CUI [14,2]
C0700589
UMLS CUI [14,3]
C0332197

Similar models

Eligibility Pre-hypertension NCT00553969

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age | Prehypertension | Borderline blood pressure | Systolic Pressure | Diastolic blood pressure | Antihypertensive therapy Redundant | Risk factor Additional Cardiovascular Disease
Item
males and females > 18 years old with pre-hypertensive or borderline blood pressures (systolic blood pressure ≥ 130 mmhg or diastolic blood pressure ≥ 85 mmhg) deemed not to need antihypertensive therapy. subjects must also have one additional risk factor for cardiovascular disease, including:
boolean
C0001779 (UMLS CUI [1])
C1696708 (UMLS CUI [2])
C1278395 (UMLS CUI [3])
C0871470 (UMLS CUI [4])
C0428883 (UMLS CUI [5])
C0585941 (UMLS CUI [6,1])
C1313915 (UMLS CUI [6,2])
C0035648 (UMLS CUI [7,1])
C1524062 (UMLS CUI [7,2])
C0007222 (UMLS CUI [7,3])
Low density lipoprotein cholesterol measurement
Item
ldl > 130 and < 160 mg/dl
boolean
C0202117 (UMLS CUI [1])
High density lipoprotein measurement
Item
hdl < 40 mg/dl
boolean
C0392885 (UMLS CUI [1])
Fasting Blood Sugar Measurement
Item
fasting blood sugar >100 and < 126 mg/dl
boolean
C2825162 (UMLS CUI [1])
Body mass index
Item
body mass index ≥ 30
boolean
C1305855 (UMLS CUI [1])
Tobacco use
Item
smoker
boolean
C0543414 (UMLS CUI [1])
Family history Premature Heart disease | FH: Hypertension
Item
family history of premature heart disease or hypertension
boolean
C0241889 (UMLS CUI [1,1])
C2749803 (UMLS CUI [1,2])
C0455405 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Cardiac event | Cerebral disorder | Vascular Diseases | Adrenergic beta-Antagonists | ACE Inhibitors | Intolerance to Adrenergic beta-Antagonists | Intolerance to ACE Inhibitors | Intolerance Suspected Adrenergic beta-Antagonists | Intolerance Suspected ACE Inhibitors | Angiotensin II receptor antagonist | Diabetes Mellitus | Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent
Item
patients with a history of cardiac, cerebral or other vascular events within the previous 6 months will be excluded. other exclusions include background therapy with a beta blocker or ace inhibitor therapy, known or suspected intolerance to beta blockers or ace inhibitors, angiotensin receptor blocker therapy, or diabetes. pregnant or lactating women, and women of child-bearing age who are not using an acceptable form of contraception are also excluded from this study.
boolean
C0741923 (UMLS CUI [1])
C0234387 (UMLS CUI [2])
C0042373 (UMLS CUI [3])
C0001645 (UMLS CUI [4])
C0003015 (UMLS CUI [5])
C1744706 (UMLS CUI [6,1])
C0001645 (UMLS CUI [6,2])
C1744706 (UMLS CUI [7,1])
C0003015 (UMLS CUI [7,2])
C1744706 (UMLS CUI [8,1])
C0750491 (UMLS CUI [8,2])
C0001645 (UMLS CUI [8,3])
C1744706 (UMLS CUI [9,1])
C0750491 (UMLS CUI [9,2])
C0003015 (UMLS CUI [9,3])
C0521942 (UMLS CUI [10])
C0011849 (UMLS CUI [11])
C0032961 (UMLS CUI [12])
C0006147 (UMLS CUI [13])
C3831118 (UMLS CUI [14,1])
C0700589 (UMLS CUI [14,2])
C0332197 (UMLS CUI [14,3])

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