ID

38744

Beschrijving

Single Oral Dose of BeneFlax to Healthy Young and Older Adults; ODM derived from: https://clinicaltrials.gov/show/NCT01531569

Link

https://clinicaltrials.gov/show/NCT01531569

Trefwoorden

Versies (1)
  1. 31-10-19 31-10-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

31 oktober 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT01531569

Engels

Eligibility Diabetes Mellitus, Type 2 NCT01531569

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy adults: 18-45 and 60-80 years of age
Beschrijving

Well adult | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0686750
UMLS CUI [2]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
Beschrijving

Strict vegetarian | Vegan | Lignans High Level

Datatype

boolean

Alias
UMLS CUI [1]
C3241968
UMLS CUI [2]
C2987738
UMLS CUI [3,1]
C0064971
UMLS CUI [3,2]
C4321237
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
Beschrijving

Strict vegetarian | Vegan | Lignans High Level

Datatype

boolean

Alias
UMLS CUI [1]
C3241968
UMLS CUI [2]
C2987738
UMLS CUI [3,1]
C0064971
UMLS CUI [3,2]
C4321237
individuals who smoke
Beschrijving

Tobacco use

Datatype

boolean

Alias
UMLS CUI [1]
C0543414
individuals who have experienced diarrhea in the last three months
Beschrijving

Diarrhea

Datatype

boolean

Alias
UMLS CUI [1]
C0011991
individuals who have taken oral antibiotics in the last three months
Beschrijving

Antidiabetics Oral

Datatype

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C1527415
individuals who are currently taking warfarin or any of its derivatives
Beschrijving

Warfarin | Warfarin Derivative

Datatype

boolean

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2,1]
C0043031
UMLS CUI [2,2]
C1527240
individuals with low haemoglobin (<121g/l for women and <137g/l for men)
Beschrijving

Hemoglobin low | Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0162119
UMLS CUI [2]
C0079399
individuals with bmi under 19 or over 28
Beschrijving

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
pregnant or lactating women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
women with child bearing potential not using contraceptives
Beschrijving

Childbearing Potential Contraceptive methods Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332197
current diagnosis of a bleeding disorder or at risk of bleeding
Beschrijving

Blood Coagulation Disorder | Bleeding risk

Datatype

boolean

Alias
UMLS CUI [1]
C0005779
UMLS CUI [2]
C3251812
individuals with gastrointestinal problems (such as ulcers), or convulsive, depressive, or hepatic disorders
Beschrijving

Gastrointestinal problem | Ulcers | Convulsive disorder | Depressive disorder | Liver diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0017187
UMLS CUI [2]
C0041582
UMLS CUI [3]
C0234972
UMLS CUI [4]
C0011581
UMLS CUI [5]
C0023895
individuals with diabetes mellitus
Beschrijving

Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
individuals currently taking a flax seed supplement
Beschrijving

Flaxseed Supplement

Datatype

boolean

Alias
UMLS CUI [1,1]
C0995001
UMLS CUI [1,2]
C0242295
individuals with an allergy to flax seed
Beschrijving

Hypersensitivity Flaxseed

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0995001
individuals who have donated blood or lost > 450 ml of blood within 56 days of study duration
Beschrijving

Blood Donation Amount Timespan | Blood Loss Amount Timespan

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005794
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0872291
UMLS CUI [2,1]
C3163616
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0872291
individuals who have participated in any other clinical trial with and investigational agent within one month of starting this trial
Beschrijving

Study Subject Participation Status | Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
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Similar models

Eligibility Diabetes Mellitus, Type 2 NCT01531569

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Well adult | Age
Item
healthy adults: 18-45 and 60-80 years of age
boolean
C0686750 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Strict vegetarian | Vegan | Lignans High Level
Item
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
boolean
C3241968 (UMLS CUI [1])
C2987738 (UMLS CUI [2])
C0064971 (UMLS CUI [3,1])
C4321237 (UMLS CUI [3,2])
Strict vegetarian | Vegan | Lignans High Level
Item
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
boolean
C3241968 (UMLS CUI [1])
C2987738 (UMLS CUI [2])
C0064971 (UMLS CUI [3,1])
C4321237 (UMLS CUI [3,2])
Tobacco use
Item
individuals who smoke
boolean
C0543414 (UMLS CUI [1])
Diarrhea
Item
individuals who have experienced diarrhea in the last three months
boolean
C0011991 (UMLS CUI [1])
Antidiabetics Oral
Item
individuals who have taken oral antibiotics in the last three months
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Warfarin | Warfarin Derivative
Item
individuals who are currently taking warfarin or any of its derivatives
boolean
C0043031 (UMLS CUI [1])
C0043031 (UMLS CUI [2,1])
C1527240 (UMLS CUI [2,2])
Hemoglobin low | Gender
Item
individuals with low haemoglobin (<121g/l for women and <137g/l for men)
boolean
C0162119 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Body mass index
Item
individuals with bmi under 19 or over 28
boolean
C1305855 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Absent
Item
women with child bearing potential not using contraceptives
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Blood Coagulation Disorder | Bleeding risk
Item
current diagnosis of a bleeding disorder or at risk of bleeding
boolean
C0005779 (UMLS CUI [1])
C3251812 (UMLS CUI [2])
Gastrointestinal problem | Ulcers | Convulsive disorder | Depressive disorder | Liver diseases
Item
individuals with gastrointestinal problems (such as ulcers), or convulsive, depressive, or hepatic disorders
boolean
C0017187 (UMLS CUI [1])
C0041582 (UMLS CUI [2])
C0234972 (UMLS CUI [3])
C0011581 (UMLS CUI [4])
C0023895 (UMLS CUI [5])
Diabetes Mellitus
Item
individuals with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Flaxseed Supplement
Item
individuals currently taking a flax seed supplement
boolean
C0995001 (UMLS CUI [1,1])
C0242295 (UMLS CUI [1,2])
Hypersensitivity Flaxseed
Item
individuals with an allergy to flax seed
boolean
C0020517 (UMLS CUI [1,1])
C0995001 (UMLS CUI [1,2])
Blood Donation Amount Timespan | Blood Loss Amount Timespan
Item
individuals who have donated blood or lost > 450 ml of blood within 56 days of study duration
boolean
C0005794 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
C3163616 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0872291 (UMLS CUI [2,3])
Study Subject Participation Status | Investigational New Drugs
Item
individuals who have participated in any other clinical trial with and investigational agent within one month of starting this trial
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
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