ID

14520

Description

Cohort Study of the Patterns of Microvesicles in the Serum of Participants With Atopic and Non-atopic Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT00700726

Link

https://clinicaltrials.gov/show/NCT00700726

Keywords

Versions (1)
  1. 4/19/16 4/19/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

April 19, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00700726

English

Eligibility Asthma NCT00700726

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00700726
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
be between the ages of 18 and 50.
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
have diagnosed asthma.
Description

asthma

Data type

boolean

Alias
UMLS CUI [1]
C0004096
must have less "one pack per day for 10 years" smoking history
Description

smoking history

Data type

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
you have had a fever of 100.4º within 24 hours of visit 2.
Description

fever

Data type

boolean

Alias
UMLS CUI [1,1]
C0015967
UMLS CUI [1,2]
C0040223
you are enrolled in another interventional research trial.
Description

enrolled in another interventional research trial

Data type

boolean

Alias
UMLS CUI [1]
C2348568
have other major chronic illnesses that would interfere with participation in the study.
Description

comorbidity limiting study participation

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
you are pregnant.
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
you chronically use oral corticosteroids.
Description

oral corticosteroids

Data type

boolean

Alias
UMLS CUI [1]
C0001617
you have taken anti-coagulants, insulin, and any investigative drugs within 2 months.
Description

anti-coagulants, insulin, and any investigative drugs

Data type

boolean

Alias
UMLS CUI [1]
C0003280
UMLS CUI [2]
C0021641
UMLS CUI [3]
C0013230
UMLS CUI [4]
C0040223
you have the inability or unwillingness to provide consent.
Description

inability or unwillingness to provide consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
inability to perform aerobic exercise.
Description

aerobic exercise

Data type

boolean

Alias
UMLS CUI [1]
C0001701
inability to perform baseline measurements.
Description

baseline measurements

Data type

boolean

Alias
UMLS CUI [1]
C1321605
less than 80% completion of screening period diaries.
Description

ompletion of screening period diaries

Data type

boolean

Alias
UMLS CUI [1,1]
C1554962
UMLS CUI [1,2]
C0376660
inability to be contacted by telephone.
Description

telephone

Data type

boolean

Alias
UMLS CUI [1]
C0039457
intention to move out of the area within 6 months.
Description

intention to move out

Data type

boolean

Alias
UMLS CUI [1]
C1299988
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Similar models

Eligibility Asthma NCT00700726

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00700726
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
be between the ages of 18 and 50.
boolean
C0001779 (UMLS CUI [1])
asthma
Item
have diagnosed asthma.
boolean
C0004096 (UMLS CUI [1])
smoking history
Item
must have less "one pack per day for 10 years" smoking history
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
fever
Item
you have had a fever of 100.4º within 24 hours of visit 2.
boolean
C0015967 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
enrolled in another interventional research trial
Item
you are enrolled in another interventional research trial.
boolean
C2348568 (UMLS CUI [1])
comorbidity limiting study participation
Item
have other major chronic illnesses that would interfere with participation in the study.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
pregnancy
Item
you are pregnant.
boolean
C0032961 (UMLS CUI [1])
oral corticosteroids
Item
you chronically use oral corticosteroids.
boolean
C0001617 (UMLS CUI [1])
anti-coagulants, insulin, and any investigative drugs
Item
you have taken anti-coagulants, insulin, and any investigative drugs within 2 months.
boolean
C0003280 (UMLS CUI [1])
C0021641 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
C0040223 (UMLS CUI [4])
inability or unwillingness to provide consent
Item
you have the inability or unwillingness to provide consent.
boolean
C0021430 (UMLS CUI [1])
aerobic exercise
Item
inability to perform aerobic exercise.
boolean
C0001701 (UMLS CUI [1])
baseline measurements
Item
inability to perform baseline measurements.
boolean
C1321605 (UMLS CUI [1])
ompletion of screening period diaries
Item
less than 80% completion of screening period diaries.
boolean
C1554962 (UMLS CUI [1,1])
C0376660 (UMLS CUI [1,2])
telephone
Item
inability to be contacted by telephone.
boolean
C0039457 (UMLS CUI [1])
intention to move out
Item
intention to move out of the area within 6 months.
boolean
C1299988 (UMLS CUI [1])
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