ID

29342

Description

Prognostic Value of the Circadian Pattern of Ambulatory Blood Pressure for Cardiovascular Risk Assessment; ODM derived from: https://clinicaltrials.gov/show/NCT00741585

Link

https://clinicaltrials.gov/show/NCT00741585

Keywords

Versions (1)
  1. 3/19/18 3/19/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 19, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT00741585

English

Eligibility Essential Hypertension NCT00741585

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female subjects ≥18 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
high-normal bp or essential hypertension.
Description

Blood Pressure High Normal | Essential Hypertension

Data type

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0205250
UMLS CUI [1,3]
C0205307
UMLS CUI [2]
C0085580
any subject with recommendation for evaluation with abpm according to the 2007 european guidelines.
Description

Recommendation Evaluation Ambulatory Blood Pressure Monitoring

Data type

boolean

Alias
UMLS CUI [1,1]
C0034866
UMLS CUI [1,2]
C1261322
UMLS CUI [1,3]
C0242876
informed consent to participate in the study prior to any study procedures.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known or suspected contraindications to any potential medication under investigation.
Description

Medical contraindication Investigational New Drugs | Medical contraindication Suspected Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0750491
UMLS CUI [2,3]
C0013230
shift-workers.
Description

Shift worker

Data type

boolean

Alias
UMLS CUI [1]
C0425104
inability to communicate and comply with all study requirements.
Description

Lacking Able to communicate | Protocol Compliance Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C2364293
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1299582
persons directly involved in the execution of this protocol.
Description

Persons Involvement with Study Execution

Data type

boolean

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C0681872
intolerants to the use of the abpm device.
Description

Intolerance Use of Ambulatory Blood Pressure Monitoring Device

Data type

boolean

Alias
UMLS CUI [1,1]
C0231199
UMLS CUI [1,2]
C1524063
UMLS CUI [1,3]
C0242876
UMLS CUI [1,4]
C0699733
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Similar models

Eligibility Essential Hypertension NCT00741585

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female subjects ≥18 years of age.
boolean
C0001779 (UMLS CUI [1])
Blood Pressure High Normal | Essential Hypertension
Item
high-normal bp or essential hypertension.
boolean
C0005823 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
C0205307 (UMLS CUI [1,3])
C0085580 (UMLS CUI [2])
Recommendation Evaluation Ambulatory Blood Pressure Monitoring
Item
any subject with recommendation for evaluation with abpm according to the 2007 european guidelines.
boolean
C0034866 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C0242876 (UMLS CUI [1,3])
Informed Consent
Item
informed consent to participate in the study prior to any study procedures.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Investigational New Drugs | Medical contraindication Suspected Investigational New Drugs
Item
known or suspected contraindications to any potential medication under investigation.
boolean
C1301624 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
Shift worker
Item
shift-workers.
boolean
C0425104 (UMLS CUI [1])
Lacking Able to communicate | Protocol Compliance Unable
Item
inability to communicate and comply with all study requirements.
boolean
C0332268 (UMLS CUI [1,1])
C2364293 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Persons Involvement with Study Execution
Item
persons directly involved in the execution of this protocol.
boolean
C0027361 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C0681872 (UMLS CUI [1,3])
Intolerance Use of Ambulatory Blood Pressure Monitoring Device
Item
intolerants to the use of the abpm device.
boolean
C0231199 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0242876 (UMLS CUI [1,3])
C0699733 (UMLS CUI [1,4])
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