ID

27634

Beschrijving

ROS Signaling in Endothelial Function; ODM derived from: https://clinicaltrials.gov/show/NCT01037465

Link

https://clinicaltrials.gov/show/NCT01037465

Trefwoorden

Versies (1)
  1. 23-11-17 23-11-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

23 november 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT01037465

Engels

Eligibility Cardiovascular Disease NCT01037465

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. sex: male and female subjects.
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
2. age range: 21-65 years old.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
3. disease status: no acute, chronic, or debilitating medical condition or use of prescribed medications.
Beschrijving

Medical condition Absent | Medical condition chronic Absent | Medical condition Debilitation Absent | Pharmaceutical Preparations prescribed Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0205191
UMLS CUI [2,3]
C0332197
UMLS CUI [3,1]
C3843040
UMLS CUI [3,2]
C0742985
UMLS CUI [3,3]
C0332197
UMLS CUI [4,1]
C0013227
UMLS CUI [4,2]
C0278329
UMLS CUI [4,3]
C0332197
4. willingness and ability to provide written informed consent and the ability to understand, to participate and to comply with the study requirements.
Beschrijving

Informed Consent | Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. women with a positive urine beta hcg pregnancy test and lactating women.
Beschrijving

Gender Urine pregnancy test positive Beta-HCG | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0430059
UMLS CUI [1,3]
C0106132
UMLS CUI [2]
C0006147
2. blood pressure greater than 140/90 mmhg; serum ldl cholesterol greater than 160 mg/dl; fasting blood sugar greater than 110 mg/dl.
Beschrijving

Blood Pressure | Serum LDL cholesterol measurement | Fasting Blood Sugar Measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0005823
UMLS CUI [2]
C0428474
UMLS CUI [3]
C2825162
3. history of any cigarette smoking within one year of the study.
Beschrijving

Tobacco use

Datatype

boolean

Alias
UMLS CUI [1]
C0543414
4. clinical history of any acute, chronic, or debilitating medical condition, including liver disease and peptic ulcer disease.
Beschrijving

Medical condition | Medical condition chronic | Medical condition Debilitation | Liver diseases | Peptic Ulcer

Datatype

boolean

Alias
UMLS CUI [1]
C3843040
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0205191
UMLS CUI [3,1]
C3843040
UMLS CUI [3,2]
C0742985
UMLS CUI [4]
C0023895
UMLS CUI [5]
C0030920
5. treatment with an investigational new drug within the last 30 days.
Beschrijving

Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0013230
6. history of a psychological illness or condition such as to interfere with the subject's ability to understand the requirements of the study.
Beschrijving

Mental disorders Interfere with Protocol Compliance | Mental condition Interferes with Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0525058
UMLS CUI [2,1]
C3840291
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0525058
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Similar models

Eligibility Cardiovascular Disease NCT01037465

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
1. sex: male and female subjects.
boolean
C0079399 (UMLS CUI [1])
Age
Item
2. age range: 21-65 years old.
boolean
C0001779 (UMLS CUI [1])
Medical condition Absent | Medical condition chronic Absent | Medical condition Debilitation Absent | Pharmaceutical Preparations prescribed Absent
Item
3. disease status: no acute, chronic, or debilitating medical condition or use of prescribed medications.
boolean
C3843040 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C3843040 (UMLS CUI [3,1])
C0742985 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0013227 (UMLS CUI [4,1])
C0278329 (UMLS CUI [4,2])
C0332197 (UMLS CUI [4,3])
Informed Consent | Protocol Compliance
Item
4. willingness and ability to provide written informed consent and the ability to understand, to participate and to comply with the study requirements.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Gender Urine pregnancy test positive Beta-HCG | Breast Feeding
Item
1. women with a positive urine beta hcg pregnancy test and lactating women.
boolean
C0079399 (UMLS CUI [1,1])
C0430059 (UMLS CUI [1,2])
C0106132 (UMLS CUI [1,3])
C0006147 (UMLS CUI [2])
Blood Pressure | Serum LDL cholesterol measurement | Fasting Blood Sugar Measurement
Item
2. blood pressure greater than 140/90 mmhg; serum ldl cholesterol greater than 160 mg/dl; fasting blood sugar greater than 110 mg/dl.
boolean
C0005823 (UMLS CUI [1])
C0428474 (UMLS CUI [2])
C2825162 (UMLS CUI [3])
Tobacco use
Item
3. history of any cigarette smoking within one year of the study.
boolean
C0543414 (UMLS CUI [1])
Medical condition | Medical condition chronic | Medical condition Debilitation | Liver diseases | Peptic Ulcer
Item
4. clinical history of any acute, chronic, or debilitating medical condition, including liver disease and peptic ulcer disease.
boolean
C3843040 (UMLS CUI [1])
C3843040 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C3843040 (UMLS CUI [3,1])
C0742985 (UMLS CUI [3,2])
C0023895 (UMLS CUI [4])
C0030920 (UMLS CUI [5])
Investigational New Drugs
Item
5. treatment with an investigational new drug within the last 30 days.
boolean
C0013230 (UMLS CUI [1])
Mental disorders Interfere with Protocol Compliance | Mental condition Interferes with Protocol Compliance
Item
6. history of a psychological illness or condition such as to interfere with the subject's ability to understand the requirements of the study.
boolean
C0004936 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
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