ID

43023

Beschreibung

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

Stichworte

Versionen (2)
  1. 10.01.16 10.01.16 -
  2. 17.09.21 17.09.21 -
Hochgeladen am

17. September 2021

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Asthma NCT00001759

Englisch

Eligibility Asthma NCT00001759

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00001759
Criteria
Beschreibung

Criteria

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

pregnancy test

Datentyp

boolean

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

informed consent

Datentyp

boolean

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

asthma or other lung disease

Datentyp

boolean

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

control subjects - allergy testing

Datentyp

boolean

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

Asthma by study definition

Datentyp

boolean

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

asthma subjects - allergy testing

Datentyp

boolean

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

primary medical care provider

Datentyp

boolean

subjects must weigh less than 136 kg.
Beschreibung

body weight

Datentyp

boolean

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

breast feeding

Datentyp

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.
Beschreibung

smoking history

Datentyp

boolean

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

antihistamines

Datentyp

boolean

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

coronary artery disease

Datentyp

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).
Beschreibung

Lung, autoimmune and inflammatory disease

Datentyp

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.
Beschreibung

lung infection

Datentyp

boolean

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

diabetes, glucose intolerance

Datentyp

boolean

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

allergy to methacholine

Datentyp

boolean

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

beta-adrenergic antagonists

Datentyp

boolean

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

control subjects - asthma, atopic rhinitis or atopic dermatitis

Datentyp

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.
Beschreibung

control subjects - metacholine response, fev1

Datentyp

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).
Beschreibung

asthmatic subjects - chronic bronchitis or copd

Datentyp

boolean

Alias
UMLS CUI [1]
C0008677
UMLS CUI [2]
C0024117
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Ähnliche Modelle

Eligibility Asthma NCT00001759

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00001759
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
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