ID

39378

Description

Time to Thrombocytic Inhibition After Supine and Upright Ingestion of Efient; ODM derived from: https://clinicaltrials.gov/show/NCT01365741

Link

https://clinicaltrials.gov/show/NCT01365741

Keywords

  1. 1/4/20 1/4/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 4, 2020

DOI

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License

Creative Commons BY 4.0

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Eligibility Heart Disease NCT01365741

Eligibility Heart Disease NCT01365741

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
20-30 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
healthy
Description

Healthy

Data type

boolean

Alias
UMLS CUI [1]
C3898900
male
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
ability to give informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
non-smoker
Description

Non-smoker

Data type

boolean

Alias
UMLS CUI [1]
C0337672
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known with reflux or dysphagia
Description

Reflux | Deglutition Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0232483
UMLS CUI [2]
C0011168
ingestion of medicine, beside paracetamol <14 prior to the trial
Description

Ingestion of drug | Exception Acetaminophen Quantity

Data type

boolean

Alias
UMLS CUI [1]
C3544179
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0000970
UMLS CUI [2,3]
C1265611
hematological diseases
Description

Hematological Disease

Data type

boolean

Alias
UMLS CUI [1]
C0018939
diabetes
Description

Diabetes Mellitus

Data type

boolean

Alias
UMLS CUI [1]
C0011849
known kidney disease
Description

Kidney Diseases

Data type

boolean

Alias
UMLS CUI [1]
C0022658
known liver disease
Description

Liver diseases

Data type

boolean

Alias
UMLS CUI [1]
C0023895
recent trauma
Description

Recent trauma

Data type

boolean

Alias
UMLS CUI [1]
C0332665
scheduled operation within 7 days after the trial
Description

Patient scheduled for surgery

Data type

boolean

Alias
UMLS CUI [1]
C3242215
former apoplexia
Description

Cerebrovascular accident Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0205156
known gastro-intestinal disease
Description

Gastrointestinal Diseases

Data type

boolean

Alias
UMLS CUI [1]
C0017178
weight <60 kg
Description

Body Weight

Data type

boolean

Alias
UMLS CUI [1]
C0005910

Similar models

Eligibility Heart Disease NCT01365741

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
20-30 years of age
boolean
C0001779 (UMLS CUI [1])
Healthy
Item
healthy
boolean
C3898900 (UMLS CUI [1])
Gender
Item
male
boolean
C0079399 (UMLS CUI [1])
Informed Consent
Item
ability to give informed consent
boolean
C0021430 (UMLS CUI [1])
Non-smoker
Item
non-smoker
boolean
C0337672 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Reflux | Deglutition Disorders
Item
known with reflux or dysphagia
boolean
C0232483 (UMLS CUI [1])
C0011168 (UMLS CUI [2])
Ingestion of drug | Exception Acetaminophen Quantity
Item
ingestion of medicine, beside paracetamol <14 prior to the trial
boolean
C3544179 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0000970 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
Hematological Disease
Item
hematological diseases
boolean
C0018939 (UMLS CUI [1])
Diabetes Mellitus
Item
diabetes
boolean
C0011849 (UMLS CUI [1])
Kidney Diseases
Item
known kidney disease
boolean
C0022658 (UMLS CUI [1])
Liver diseases
Item
known liver disease
boolean
C0023895 (UMLS CUI [1])
Recent trauma
Item
recent trauma
boolean
C0332665 (UMLS CUI [1])
Patient scheduled for surgery
Item
scheduled operation within 7 days after the trial
boolean
C3242215 (UMLS CUI [1])
Cerebrovascular accident Previous
Item
former apoplexia
boolean
C0038454 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Gastrointestinal Diseases
Item
known gastro-intestinal disease
boolean
C0017178 (UMLS CUI [1])
Body Weight
Item
weight <60 kg
boolean
C0005910 (UMLS CUI [1])

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