ID

43023

Descripción

Assessment of Lung Inflammation in Patients With Atopic Asthma Using Positron Emission Tomography; ODM derived from: https://clinicaltrials.gov/show/NCT00001759

Link

https://clinicaltrials.gov/show/NCT00001759

Palabras clave

Versiones (2)
  1. 10/1/16 10/1/16 -
  2. 17/9/21 17/9/21 -
Subido en

17 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Asthma NCT00001759

Inglés

Eligibility Asthma NCT00001759

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00001759
Criteria
Descripción

Criteria

negative pregnancy test within two days of the scan and willingness to adhere to reliable birth control until the completion of the protocol.
Descripción

pregnancy test

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032976
UMLS CUI [2]
C0032961
subjects must be able to give informed consent.
Descripción

informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
subjects in the negative control group must have no history of asthma or other lung disease.
Descripción

asthma or other lung disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0024115
control subjects must have negative prick skin tests to the allergens used.
Descripción

control subjects - allergy testing

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0199747
UMLS CUI [2]
C0430561
asthmatic subjects must have asthma as defined in this study.
Descripción

Asthma by study definition

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
asthmatic subjects must have positive prick skin tests to one or more allergens used.
Descripción

asthma subjects - allergy testing

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0199747
UMLS CUI [2]
C0430561
subjects must have access to a primary medical care provider outside of the nih.
Descripción

primary medical care provider

Tipo de datos

boolean

subjects must weigh less than 136 kg.
Descripción

body weight

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005910
no breast feeding.
Descripción

breast feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
no smoking in the last 3 years, or greater than 6 months of smoking in the past ten years.
Descripción

smoking history

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519384
no antihistamines one week prior to the skin test on the first visit.
Descripción

antihistamines

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019590
no history of coronary artery disease.
Descripción

coronary artery disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1956346
no evidence of lung disease other than asthma; no evidence of autoimmune or inflammatory disease which could affect lung function such as lupus erythematosus (except for the control subjects with wegener's granulomatosis).
Descripción

Lung, autoimmune and inflammatory disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024115
UMLS CUI [2]
C0004364
UMLS CUI [3]
C1290884
no evidence of either acute (e.g., bacterial or viral pneumonia) or chronic (e.g., bronchiectasis) lung infection.
Descripción

lung infection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0876973
no diabetes, or history of glucose intolerance (e.g., gestational diabetes).
Descripción

diabetes, glucose intolerance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0271650
no allergy to methacholine.
Descripción

allergy to methacholine

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0600370
no beta-adrenergic blocking medication.
Descripción

beta-adrenergic antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001645
control subjects must not have a history of asthma, atopic rhinitis or atopic dermatitis.
Descripción

control subjects - asthma, atopic rhinitis or atopic dermatitis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0002103
UMLS CUI [3]
C0011615
control subjects must not have any response to inhaled methacholine with a fall in fev1 in excess of 20% to less than or equal to 25 mg/ml.
Descripción

control subjects - metacholine response, fev1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0600370
UMLS CUI [2]
C0748133
asthmatic subjects must not have chronic bronchitis or a diagnosis of chronic obstructive lung disease (copd).
Descripción

asthmatic subjects - chronic bronchitis or copd

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0008677
UMLS CUI [2]
C0024117
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Similar models

Eligibility Asthma NCT00001759

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00001759
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
pregnancy test
Item
negative pregnancy test within two days of the scan and willingness to adhere to reliable birth control until the completion of the protocol.
boolean
C0032976 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
informed consent
Item
subjects must be able to give informed consent.
boolean
C0021430 (UMLS CUI [1])
asthma or other lung disease
Item
subjects in the negative control group must have no history of asthma or other lung disease.
boolean
C0004096 (UMLS CUI [1])
C0024115 (UMLS CUI [2])
control subjects - allergy testing
Item
control subjects must have negative prick skin tests to the allergens used.
boolean
C0199747 (UMLS CUI [1])
C0430561 (UMLS CUI [2])
Asthma by study definition
Item
asthmatic subjects must have asthma as defined in this study.
boolean
C0004096 (UMLS CUI [1])
asthma subjects - allergy testing
Item
asthmatic subjects must have positive prick skin tests to one or more allergens used.
boolean
C0199747 (UMLS CUI [1])
C0430561 (UMLS CUI [2])
primary medical care provider
Item
subjects must have access to a primary medical care provider outside of the nih.
boolean
body weight
Item
subjects must weigh less than 136 kg.
boolean
C0005910 (UMLS CUI [1])
breast feeding
Item
no breast feeding.
boolean
C0006147 (UMLS CUI [1])
smoking history
Item
no smoking in the last 3 years, or greater than 6 months of smoking in the past ten years.
boolean
C1519384 (UMLS CUI [1])
antihistamines
Item
no antihistamines one week prior to the skin test on the first visit.
boolean
C0019590 (UMLS CUI [1])
coronary artery disease
Item
no history of coronary artery disease.
boolean
C1956346 (UMLS CUI [1])
Lung, autoimmune and inflammatory disease
Item
no evidence of lung disease other than asthma; no evidence of autoimmune or inflammatory disease which could affect lung function such as lupus erythematosus (except for the control subjects with wegener's granulomatosis).
boolean
C0024115 (UMLS CUI [1])
C0004364 (UMLS CUI [2])
C1290884 (UMLS CUI [3])
lung infection
Item
no evidence of either acute (e.g., bacterial or viral pneumonia) or chronic (e.g., bronchiectasis) lung infection.
boolean
C0876973 (UMLS CUI [1])
diabetes, glucose intolerance
Item
no diabetes, or history of glucose intolerance (e.g., gestational diabetes).
boolean
C0011849 (UMLS CUI [1])
C0271650 (UMLS CUI [2])
allergy to methacholine
Item
no allergy to methacholine.
boolean
C0020517 (UMLS CUI [1,1])
C0600370 (UMLS CUI [1,2])
beta-adrenergic antagonists
Item
no beta-adrenergic blocking medication.
boolean
C0001645 (UMLS CUI [1])
control subjects - asthma, atopic rhinitis or atopic dermatitis
Item
control subjects must not have a history of asthma, atopic rhinitis or atopic dermatitis.
boolean
C0004096 (UMLS CUI [1])
C0002103 (UMLS CUI [2])
C0011615 (UMLS CUI [3])
control subjects - metacholine response, fev1
Item
control subjects must not have any response to inhaled methacholine with a fall in fev1 in excess of 20% to less than or equal to 25 mg/ml.
boolean
C0600370 (UMLS CUI [1])
C0748133 (UMLS CUI [2])
asthmatic subjects - chronic bronchitis or copd
Item
asthmatic subjects must not have chronic bronchitis or a diagnosis of chronic obstructive lung disease (copd).
boolean
C0008677 (UMLS CUI [1])
C0024117 (UMLS CUI [2])
Volver a la parte superior de la página 

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