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

Lien

https://clinicaltrials.gov/show/NCT00700726

Mots-clés

  1. 19/04/2016 19/04/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

19 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00700726

Eligibility Asthma NCT00700726

  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

Type de données

boolean

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

asthma

Type de données

boolean

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

smoking history

Type de données

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

Type de données

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

Type de données

boolean

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

comorbidity limiting study participation

Type de données

boolean

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

pregnancy

Type de données

boolean

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

oral corticosteroids

Type de données

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

Type de données

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

Type de données

boolean

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

aerobic exercise

Type de données

boolean

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

baseline measurements

Type de données

boolean

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

ompletion of screening period diaries

Type de données

boolean

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

telephone

Type de données

boolean

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

intention to move out

Type de données

boolean

Alias
UMLS CUI [1]
C1299988

Similar models

Eligibility Asthma NCT00700726

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00700726
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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