ID

36660

Beschreibung

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

Stichworte

Versionen (3)
  1. 17.01.19 17.01.19 -
  2. 27.05.19 27.05.19 -
  3. 29.05.19 29.05.19 -
Rechteinhaber

University of Oslo

Hochgeladen am

29. Mai 2019

DOI

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Lizenz

Creative Commons BY-NC 3.0
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Polyphenol-rich Berry Juice in Hypertension NCT01568983

Englisch

Eligibility Criteria

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Beschreibung

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)
Beschreibung

Pre-hypertension or hypertension (blood pressure ranges)

Datentyp

boolean

Alias
UMLS CUI [1]
C1696708
UMLS CUI [2]
C0020538
UMLS CUI [3]
C0871470
UMLS CUI [4]
C0428883
bmi 20-35 kg/m2
Beschreibung

BMI

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
stable weight (change <4 kg previous 12 weeks)
Beschreibung

recent stable weight

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0517386
UMLS CUI [1,2]
C0332185
Patients aged 50 - 70 years
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
regular use of blood pressure lowering agents
Beschreibung

regular blood pressure lowering medication

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0205272
diabetes type I or II
Beschreibung

diabetes type I or II

Datentyp

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
smokers
Beschreibung

smokers

Datentyp

boolean

Alias
UMLS CUI [1]
C0543414
allergy to grape, cherries, blueberries/bilberries, black currant, aronia
Beschreibung

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

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0016470
UMLS CUI [1,2]
C0018208
UMLS CUI [2]
C1636184
UMLS CUI [3,1]
C0016470
UMLS CUI [3,2]
C0950037
UMLS CUI [4,1]
C0016470
UMLS CUI [4,2]
C0936049
UMLS CUI [5,1]
C0016470
UMLS CUI [5,2]
C0453277
UMLS CUI [6,1]
C0016470
UMLS CUI [6,2]
C1215581
supplements for weight loss
Beschreibung

supplements for weight loss

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0376606
UMLS CUI [1,2]
C0242295
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)
Beschreibung

changes in pharmacological treatment of hyperlipidemia or hyperglycemia, recently or during study

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0392747
UMLS CUI [1,3]
C0020473
UMLS CUI [1,4]
C0332185
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C0392747
UMLS CUI [2,3]
C0020456
UMLS CUI [2,4]
C0332185
UMLS CUI [3,1]
C0013216
UMLS CUI [3,2]
C0392747
UMLS CUI [3,3]
C0020473
UMLS CUI [3,4]
C0489652
UMLS CUI [4,1]
C0013216
UMLS CUI [4,2]
C0392747
UMLS CUI [4,3]
C0020456
UMLS CUI [4,4]
C0489652
participation in a drug trial during the previous 30 days
Beschreibung

recent participation in a drug trial

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0013216
UMLS CUI [1,3]
C0332185
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Ähnliche Modelle

Eligibility Criteria

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Pre-hypertension or hypertension (blood pressure ranges)
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
C1696708 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
C0428883 (UMLS CUI [4])
BMI
Item
bmi 20-35 kg/m2
boolean
C1305855 (UMLS CUI [1])
recent stable weight
Item
stable weight (change <4 kg previous 12 weeks)
boolean
C0517386 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Age
Item
Patients aged 50 - 70 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
regular blood pressure lowering medication
Item
regular use of blood pressure lowering agents
boolean
C0003364 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
diabetes type I or II
Item
diabetes type I or II
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
smokers
Item
smokers
boolean
C0543414 (UMLS CUI [1])
allergy to grape, cherries, blueberries/bilberries, black currant, aronia
Item
allergy to grape, cherries, blueberries/bilberries, black currant, aronia
boolean
C0016470 (UMLS CUI [1,1])
C0018208 (UMLS CUI [1,2])
C1636184 (UMLS CUI [2])
C0016470 (UMLS CUI [3,1])
C0950037 (UMLS CUI [3,2])
C0016470 (UMLS CUI [4,1])
C0936049 (UMLS CUI [4,2])
C0016470 (UMLS CUI [5,1])
C0453277 (UMLS CUI [5,2])
C0016470 (UMLS CUI [6,1])
C1215581 (UMLS CUI [6,2])
supplements for weight loss
Item
supplements for weight loss
boolean
C0376606 (UMLS CUI [1,1])
C0242295 (UMLS CUI [1,2])
changes in pharmacological treatment of hyperlipidemia or hyperglycemia, recently or during study
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
C0013216 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C0020473 (UMLS CUI [1,3])
C0332185 (UMLS CUI [1,4])
C0013216 (UMLS CUI [2,1])
C0392747 (UMLS CUI [2,2])
C0020456 (UMLS CUI [2,3])
C0332185 (UMLS CUI [2,4])
C0013216 (UMLS CUI [3,1])
C0392747 (UMLS CUI [3,2])
C0020473 (UMLS CUI [3,3])
C0489652 (UMLS CUI [3,4])
C0013216 (UMLS CUI [4,1])
C0392747 (UMLS CUI [4,2])
C0020456 (UMLS CUI [4,3])
C0489652 (UMLS CUI [4,4])
recent participation in a drug trial
Item
participation in a drug trial during the previous 30 days
boolean
C2348568 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
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