ID

33684

Description

Nighttime Dosing of Antihypertensive Drugs in Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01158625

Lien

https://clinicaltrials.gov/show/NCT01158625

Mots-clés

  1. 19/12/2018 19/12/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

19 décembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Diabetes Mellitus, Type 2 NCT01158625

Eligibility Diabetes Mellitus, Type 2 NCT01158625

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes
Description

Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
systolic nighttime blood pressure above 120 mm hg
Description

Systolic Pressure Night time

Type de données

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0240526
systolic daytime blood pressure not exceeding 150 mm hg
Description

Systolic Pressure Daytime

Type de données

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0332169
antihypertensive treatment which must include
Description

Antihypertensive therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0585941
once-daily drugs
Description

Pharmaceutical Preparations Once daily

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0556983
at least one drug must be a angiotensin-converting enzyme inhibitor, angiotensin ii receptor blocker or renin inhibitor.
Description

Angiotensin-Converting Enzyme Inhibitors Quantity | Angiotensin II receptor antagonist Quantity | Renin inhibitor Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C0521942
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C1960108
UMLS CUI [3,2]
C1265611
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
mi or stroke within 6 months
Description

Myocardial Infarction | Cerebrovascular accident

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
heart failure (ef < 45 %)
Description

Heart failure | Cardiac ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C0232174
atrial fibrillation
Description

Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
egfr < 30 ml/min
Description

Estimated Glomerular Filtration Rate

Type de données

boolean

Alias
UMLS CUI [1]
C3811844

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT01158625

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Systolic Pressure Night time
Item
systolic nighttime blood pressure above 120 mm hg
boolean
C0871470 (UMLS CUI [1,1])
C0240526 (UMLS CUI [1,2])
Systolic Pressure Daytime
Item
systolic daytime blood pressure not exceeding 150 mm hg
boolean
C0871470 (UMLS CUI [1,1])
C0332169 (UMLS CUI [1,2])
Antihypertensive therapy
Item
antihypertensive treatment which must include
boolean
C0585941 (UMLS CUI [1])
Pharmaceutical Preparations Once daily
Item
once-daily drugs
boolean
C0013227 (UMLS CUI [1,1])
C0556983 (UMLS CUI [1,2])
Angiotensin-Converting Enzyme Inhibitors Quantity | Angiotensin II receptor antagonist Quantity | Renin inhibitor Quantity
Item
at least one drug must be a angiotensin-converting enzyme inhibitor, angiotensin ii receptor blocker or renin inhibitor.
boolean
C0003015 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0521942 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C1960108 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction | Cerebrovascular accident
Item
mi or stroke within 6 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Heart failure | Cardiac ejection fraction
Item
heart failure (ef < 45 %)
boolean
C0018801 (UMLS CUI [1])
C0232174 (UMLS CUI [2])
Atrial Fibrillation
Item
atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
egfr < 30 ml/min
boolean
C3811844 (UMLS CUI [1])

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