ID

25960

Description

Bioavailability and Metabolism of Anthocyanins Following Acute Cranberry Consumption; ODM derived from: https://clinicaltrials.gov/show/NCT00809900

Link

https://clinicaltrials.gov/show/NCT00809900

Keywords

Versions (3)
  1. 10/2/17 10/2/17 -
  2. 10/4/17 10/4/17 -
  3. 10/22/17 10/22/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 2, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Bioavailability NCT00809900

English

Eligibility Bioavailability NCT00809900

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
stable cad patients
Description

Coronary Artery Disease Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0205360
men & postmenopausal women
Description

Gender | Postmenopausal state

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0232970
aged 21-80 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
all ethnic groups
Description

Ethnic groups All

Data type

boolean

Alias
UMLS CUI [1,1]
C0015031
UMLS CUI [1,2]
C0444868
english language
Description

English Language

Data type

boolean

Alias
UMLS CUI [1]
C0376245
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with heart failure are not eligible for participation in this study.
Description

Heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018801
women with a positive urine beta hcg pregnancy test and lactating women or women who are planning to become pregnant.
Description

Pregnancy test Urine beta human chorionic gonadotropin positive | Breast Feeding | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0032976
UMLS CUI [1,2]
C1737232
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
clinical history of other major illness including end-stage cancer, renal failure, hepatic failure, gastrointestinal disorders that may impair absorption, or other conditions that in the opinion of the principal investigator make a clinical study inappropriate.
Description

Illness Major | End stage cancer | Kidney Failure | Liver Failure | Gastrointestinal Diseases Impairing Absorption | Condition Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205164
UMLS CUI [2]
C0741884
UMLS CUI [3]
C0035078
UMLS CUI [4]
C0085605
UMLS CUI [5,1]
C0017178
UMLS CUI [5,2]
C0221099
UMLS CUI [5,3]
C0237442
UMLS CUI [6,1]
C0348080
UMLS CUI [6,2]
C2348568
UMLS CUI [6,3]
C1548788
regular use of oral steroids
Description

Steroids Oral Use Regular

Data type

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C1527415
UMLS CUI [1,3]
C1524063
UMLS CUI [1,4]
C0205272
cigarette smoking and/or nicotine replacement use
Description

Cigarette smoker | Nicotine Replacement Use of

Data type

boolean

Alias
UMLS CUI [1]
C0337667
UMLS CUI [2,1]
C0028040
UMLS CUI [2,2]
C0559956
UMLS CUI [2,3]
C1524063
regular daily intake of ≥ 2 alcoholic drinks
Description

Alcoholic drinks Quantity Daily

Data type

boolean

Alias
UMLS CUI [1,1]
C0001967
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0332173
illicit drug use
Description

Illicit drug use

Data type

boolean

Alias
UMLS CUI [1]
C0281875
history of a psychological illness or condition such as to interfere with the subject's ability to understand the requirements of the study.
Description

Psychological disease Interferes with Comprehension Study Protocol | Condition Interferes with Comprehension Study Protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C1658764
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0162340
UMLS CUI [1,4]
C2348563
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C2348563
no dietary supplements containing phenolic compounds, i.e., herbal preparations, or berry containing preparations (such as cranberry capsules) for one month prior to study admission.
Description

Dietary Supplements Containing Phenolics | Plant Preparations | Berry preparation | Cranberry preparation

Data type

boolean

Alias
UMLS CUI [1,1]
C0242295
UMLS CUI [1,2]
C0332256
UMLS CUI [1,3]
C0359916
UMLS CUI [2]
C0949854
UMLS CUI [3]
C3495134
UMLS CUI [4]
C0453273
treatment with an investigational new drug within the last 30 days.
Description

Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013230
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Similar models

Eligibility Bioavailability NCT00809900

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Coronary Artery Disease Stable
Item
stable cad patients
boolean
C1956346 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Gender | Postmenopausal state
Item
men & postmenopausal women
boolean
C0079399 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
Age
Item
aged 21-80 years
boolean
C0001779 (UMLS CUI [1])
Ethnic groups All
Item
all ethnic groups
boolean
C0015031 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
English Language
Item
english language
boolean
C0376245 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Heart failure
Item
subjects with heart failure are not eligible for participation in this study.
boolean
C0018801 (UMLS CUI [1])
Pregnancy test Urine beta human chorionic gonadotropin positive | Breast Feeding | Pregnancy, Planned
Item
women with a positive urine beta hcg pregnancy test and lactating women or women who are planning to become pregnant.
boolean
C0032976 (UMLS CUI [1,1])
C1737232 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Illness Major | End stage cancer | Kidney Failure | Liver Failure | Gastrointestinal Diseases Impairing Absorption | Condition Study Subject Participation Status Inappropriate
Item
clinical history of other major illness including end-stage cancer, renal failure, hepatic failure, gastrointestinal disorders that may impair absorption, or other conditions that in the opinion of the principal investigator make a clinical study inappropriate.
boolean
C0221423 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0741884 (UMLS CUI [2])
C0035078 (UMLS CUI [3])
C0085605 (UMLS CUI [4])
C0017178 (UMLS CUI [5,1])
C0221099 (UMLS CUI [5,2])
C0237442 (UMLS CUI [5,3])
C0348080 (UMLS CUI [6,1])
C2348568 (UMLS CUI [6,2])
C1548788 (UMLS CUI [6,3])
Steroids Oral Use Regular
Item
regular use of oral steroids
boolean
C0038317 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C1524063 (UMLS CUI [1,3])
C0205272 (UMLS CUI [1,4])
Cigarette smoker | Nicotine Replacement Use of
Item
cigarette smoking and/or nicotine replacement use
boolean
C0337667 (UMLS CUI [1])
C0028040 (UMLS CUI [2,1])
C0559956 (UMLS CUI [2,2])
C1524063 (UMLS CUI [2,3])
Alcoholic drinks Quantity Daily
Item
regular daily intake of ≥ 2 alcoholic drinks
boolean
C0001967 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0332173 (UMLS CUI [1,3])
Illicit drug use
Item
illicit drug use
boolean
C0281875 (UMLS CUI [1])
Psychological disease Interferes with Comprehension Study Protocol | Condition Interferes with Comprehension Study Protocol
Item
history of a psychological illness or condition such as to interfere with the subject's ability to understand the requirements of the study.
boolean
C1658764 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
Dietary Supplements Containing Phenolics | Plant Preparations | Berry preparation | Cranberry preparation
Item
no dietary supplements containing phenolic compounds, i.e., herbal preparations, or berry containing preparations (such as cranberry capsules) for one month prior to study admission.
boolean
C0242295 (UMLS CUI [1,1])
C0332256 (UMLS CUI [1,2])
C0359916 (UMLS CUI [1,3])
C0949854 (UMLS CUI [2])
C3495134 (UMLS CUI [3])
C0453273 (UMLS CUI [4])
Investigational New Drugs
Item
treatment with an investigational new drug within the last 30 days.
boolean
C0013230 (UMLS CUI [1])
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