Information:
Error:
ID
14478
Description
A Study of Healthy Subjects to Assess the Effect of LY450139 on Amyloid Beta Peptide Production Rate and or Dose Response.; ODM derived from: https://clinicaltrials.gov/show/NCT00765115
Link
https://clinicaltrials.gov/show/NCT00765115
Keywords
Versions (1)
- 4/17/16 4/17/16 -
Uploaded on
April 17, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Alzheimer Disease NCT00765115
Eligibility Alzheimer Disease NCT00765115
- StudyEvent: Eligibility
Similar models
Eligibility Alzheimer Disease NCT00765115
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
healthy volunteers; men; age
Item
healthy volunteers: men within the ages of 21 and 50
boolean
C1708335 (UMLS CUI [1])
C0025266 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0025266 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
Compliance behavior Limited Comorbidity
Item
have serious or unstable medical conditions
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
head trauma; unconsciousness
Item
have a history of serious infections affecting the brain or head trauma resulting in protracted loss of consciousness within the last 5 years or multiple episodes of head trauma
boolean
C0018674 (UMLS CUI [1])
C0041657 (UMLS CUI [2])
C0041657 (UMLS CUI [2])
malignant disease
Item
have a history of primary or recurrent malignant disease
boolean
C0006826 (UMLS CUI [1])
laboratory test abnormal
Item
have a recent laboratory result indicating a clinically significant laboratory abnormality as determined by the investigator
boolean
C0022885 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
Substance Use Disorder
Item
have a history of chronic alcohol or drug abuse within the past 5 years
boolean
C0038586 (UMLS CUI [1])
human immunodeficiency virus; afebrile seizures; Drug Allergy
Item
have a known history of human immunodeficiency virus (hiv), afebrile seizures, or clinically significant multiple drug allergies
boolean
C0019682 (UMLS CUI [1])
C0863106 (UMLS CUI [2])
C0013182 (UMLS CUI [3])
C0863106 (UMLS CUI [2])
C0013182 (UMLS CUI [3])
suicidal
Item
are judged clinically by the investigator to be at serious risk for suicide
boolean
C0438696 (UMLS CUI [1])
electrocardiogram
Item
have electrocardiogram abnormalities obtained at visit 1 that in the opinion of the investigator are clinically significant
boolean
C0013798 (UMLS CUI [1])
concomitant medication
Item
use of prescription or over the counter medications that cannot safely be discontinued within 14 days prior to visit 2
boolean
C2347852 (UMLS CUI [1])
hypersensitivity local anesthetics; local infection
Item
have criteria that would preclude a lp such as allergy to all local anesthetics; have a local infection at the site of the lp or have any medical condition requiring treatment with warfarin or heparin.
boolean
C0020517 (UMLS CUI [1,1])
C0002921 (UMLS CUI [1,2])
C1400591 (UMLS CUI [2])
C0002921 (UMLS CUI [1,2])
C1400591 (UMLS CUI [2])
Study Subject Participation Status
Item
have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
boolean
C2348568 (UMLS CUI [1])
investigator
Item
are investigator site personnel directly affiliated with this study and or immediate families.
boolean
C2826892 (UMLS CUI [1])
employees
Item
are lilly employees
boolean
C0599987 (UMLS CUI [1])