ID

14534

Description

Wheeze Detection in Adults During Dynamic Bronchial Situations Measured by PulmoTrack® 2010 With WIM-PC™ Technologies Recording; ODM derived from: https://clinicaltrials.gov/show/NCT00644462

Lien

https://clinicaltrials.gov/show/NCT00644462

Mots-clés

  1. 19/04/2016 19/04/2016 -
Téléchargé le

19 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Asthma, Bronchial NCT00644462

Eligibility Asthma, Bronchial NCT00644462

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
asthmatic or healthy subjects;
Description

Asthma | Healthy Subjects

Type de données

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C1708335
age 18 and up;
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
not smoking for at the last two years;
Description

Cessation of smoking

Type de données

boolean

Alias
UMLS CUI [1]
C0085134
subject or subject's parents/guardian is able to comprehend and give informed consent for participation in the study.
Description

Informed Consent | parent | Guardian

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0030551
UMLS CUI [3]
C1274041
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
chest burns;
Description

Chest burning

Type de données

boolean

Alias
UMLS CUI [1]
C0740396
copd;
Description

Chronic Obstructive Airway Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0024117
pregnant or lactating;
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
mechanically ventilatory;
Description

Mechanical Ventilator

Type de données

boolean

Alias
UMLS CUI [1]
C0042497
homodynamic instability;
Description

Hemodynamic instability

Type de données

boolean

Alias
UMLS CUI [1]
C0948268
unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to screening;
Description

Angina, Unstable | Congestive heart failure | Hospitalization

Type de données

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0018802
UMLS CUI [3]
C0019993
acute infection requiring intravenous antibiotics at the time of screening;
Description

Acute infectious disease | Intravenous antibiotic therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0275518
UMLS CUI [2]
C0559680
uncontrolled bleeding and coagulation disorders;
Description

Bleeding uncontrolled | Blood Coagulation Disorders

Type de données

boolean

Alias
UMLS CUI [1]
C3842135
UMLS CUI [2]
C0005779
uncontrolled diabetes mellitus: iddm or niddm;
Description

Diabetic - poor control | Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0421258
UMLS CUI [2]
C0011854
UMLS CUI [3]
C0011860
hiv positive or any other immunosuppressive disorder;
Description

HIV Seropositivity | Immune System Diseases

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0021053
subject objects to the study protocol;
Description

Study Protocol Disapproved

Type de données

boolean

Alias
UMLS CUI [1]
C2347711
concurrent participation in any other clinical study;
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
physician objection.
Description

Physician Dissent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0031831
UMLS CUI [1,2]
C0012742

Similar models

Eligibility Asthma, Bronchial NCT00644462

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Asthma | Healthy Subjects
Item
asthmatic or healthy subjects;
boolean
C0004096 (UMLS CUI [1])
C1708335 (UMLS CUI [2])
Age
Item
age 18 and up;
boolean
C0001779 (UMLS CUI [1])
Cessation of smoking
Item
not smoking for at the last two years;
boolean
C0085134 (UMLS CUI [1])
Informed Consent | parent | Guardian
Item
subject or subject's parents/guardian is able to comprehend and give informed consent for participation in the study.
boolean
C0021430 (UMLS CUI [1])
C0030551 (UMLS CUI [2])
C1274041 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Chest burning
Item
chest burns;
boolean
C0740396 (UMLS CUI [1])
Chronic Obstructive Airway Disease
Item
copd;
boolean
C0024117 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Mechanical Ventilator
Item
mechanically ventilatory;
boolean
C0042497 (UMLS CUI [1])
Hemodynamic instability
Item
homodynamic instability;
boolean
C0948268 (UMLS CUI [1])
Angina, Unstable | Congestive heart failure | Hospitalization
Item
unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to screening;
boolean
C0002965 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
C0019993 (UMLS CUI [3])
Acute infectious disease | Intravenous antibiotic therapy
Item
acute infection requiring intravenous antibiotics at the time of screening;
boolean
C0275518 (UMLS CUI [1])
C0559680 (UMLS CUI [2])
Bleeding uncontrolled | Blood Coagulation Disorders
Item
uncontrolled bleeding and coagulation disorders;
boolean
C3842135 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
Diabetic - poor control | Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
uncontrolled diabetes mellitus: iddm or niddm;
boolean
C0421258 (UMLS CUI [1])
C0011854 (UMLS CUI [2])
C0011860 (UMLS CUI [3])
HIV Seropositivity | Immune System Diseases
Item
hiv positive or any other immunosuppressive disorder;
boolean
C0019699 (UMLS CUI [1])
C0021053 (UMLS CUI [2])
Study Protocol Disapproved
Item
subject objects to the study protocol;
boolean
C2347711 (UMLS CUI [1])
Study Subject Participation Status
Item
concurrent participation in any other clinical study;
boolean
C2348568 (UMLS CUI [1])
Physician Dissent
Item
physician objection.
boolean
C0031831 (UMLS CUI [1,1])
C0012742 (UMLS CUI [1,2])

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