ID

34467

Beschrijving

The Effects of Polyphenol-rich Berry Juice on Blood Pressure in Hypertensive Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT01568983

Link

https://clinicaltrials.gov/show/NCT01568983

Trefwoorden

  1. 17-01-19 17-01-19 -
  2. 27-05-19 27-05-19 -
  3. 29-05-19 29-05-19 -
Houder van rechten

GSK group of companies

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Pre-hypertension NCT01568983

Eligibility Pre-hypertension NCT01568983

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
pre-hypertension or hypertension systolic blood pressure in the 130-179 mmhg range and/or diastolic blood pressure in the 85-109 mmhg range)
Beschrijving

ID.1

Datatype

boolean

bmi 20-35 kg/m2
Beschrijving

ID.2

Datatype

boolean

stable weight (change <4 kg previous 12 weeks)
Beschrijving

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
regular use of blood pressure lowering agens
Beschrijving

ID.4

Datatype

boolean

diabetes type i or ii
Beschrijving

ID.5

Datatype

boolean

smokers
Beschrijving

ID.6

Datatype

boolean

allergy to grape, cherries, blueberries/bilberries, black currant, aronia
Beschrijving

ID.7

Datatype

boolean

supplements for weight loss
Beschrijving

ID.8

Datatype

boolean

changes in pharmacological treatment of hyperlipidemia or hyperglycemia (initiation, termination or changes in dosage) last 30 days prior to inclusion or during the study period (run-in and intervention)
Beschrijving

ID.9

Datatype

boolean

participation in a drug trial during the previous 30 days
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Pre-hypertension NCT01568983

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
pre-hypertension or hypertension systolic blood pressure in the 130-179 mmhg range and/or diastolic blood pressure in the 85-109 mmhg range)
boolean
ID.2
Item
bmi 20-35 kg/m2
boolean
ID.3
Item
stable weight (change <4 kg previous 12 weeks)
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
regular use of blood pressure lowering agens
boolean
ID.5
Item
diabetes type i or ii
boolean
ID.6
Item
smokers
boolean
ID.7
Item
allergy to grape, cherries, blueberries/bilberries, black currant, aronia
boolean
ID.8
Item
supplements for weight loss
boolean
ID.9
Item
changes in pharmacological treatment of hyperlipidemia or hyperglycemia (initiation, termination or changes in dosage) last 30 days prior to inclusion or during the study period (run-in and intervention)
boolean
ID.10
Item
participation in a drug trial during the previous 30 days
boolean

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