ID

14139

Beschreibung

Clinical Assessment of Acupuncture for the Treatment of Chronic Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT01931696

Link

https://clinicaltrials.gov/show/NCT01931696

Stichworte

Versionen (1)
  1. 31.03.16 31.03.16 -
Hochgeladen am

31. März 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Asthma NCT01931696

Englisch

Eligibility Asthma NCT01931696

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01931696
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients diagnosed with mild-to-moderate persistent asthma
Beschreibung

Mild persistent asthma | Moderate persistent asthma

Datentyp

boolean

Alias
UMLS CUI [1]
C1960046
UMLS CUI [2]
C1960047
forced expiratory volume in one second (fev1) reversibility of greater than or equal to 12% following bronchodilator administration (2 puffs)
Beschreibung

Forced Expiratory Volume in 1 Second Reversibility | post bronchodilator

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3830088
UMLS CUI [1,2]
C2599594
patients who have given written informed consent
Beschreibung

Informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
participation in another clinical trial 1 month prior to study entry
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
use of systemic corticosteroids 2 weeks prior to study entry
Beschreibung

Systemic steroids | Use of

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2825233
UMLS CUI [1,2]
C1524063
patients with general infection, lower respiratory infection, pulmonary tuberculosis and fungal infection 1 month prior to study entry
Beschreibung

Communicable Diseases | Lower respiratory tract infection | Tuberculosis, Pulmonary | Mycoses

Datentyp

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0149725
UMLS CUI [3]
C0041327
UMLS CUI [4]
C0026946
hospitalization due to acute exacerbation 3 months prior to study entry
Beschreibung

Hospitalization | exacerbation acute

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0743630
patients cannot stop using forbidden drugs which include inhaled corticosteroid, theophylline, long-term β2 agonist, sodium cromoglicate, leukotrienes antagonist and anticholinergic drug
Beschreibung

Inhaled steroids | Theophylline | Adrenergic beta-2 Receptor Agonists | Cromolyn Sodium | Leukotriene Antagonists | Anticholinergic Agents

Datentyp

boolean

Alias
UMLS CUI [1]
C2065041
UMLS CUI [2]
C0039771
UMLS CUI [3]
C2936789
UMLS CUI [4]
C0012694
UMLS CUI [5]
C0595726
UMLS CUI [6]
C0242896
patients who are allergic to albuterol and corticosteroid
Beschreibung

Hypersensitivity | Albuterol | Adrenal Cortex Hormones

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0001927
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0001617
patients with severe primary diseases such as cancer, cardiovascular system, liver, kidney and hematopoietic system diseases
Beschreibung

Malignant Neoplasms | Cardiovascular Diseases | Liver diseases | Kidney Diseases | Hematological Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0007222
UMLS CUI [3]
C0023895
UMLS CUI [4]
C0022658
UMLS CUI [5]
C0018939
wheeze caused by pulmonary tuberculosis, bronchiectasia and cardiac insufficiency
Beschreibung

Wheeze | Tuberculosis, Pulmonary | Bronchiectasis | Heart failure

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0035508
UMLS CUI [1,2]
C0041327
UMLS CUI [2]
C0006267
UMLS CUI [3]
C0018801
patients with hyperthyroidism
Beschreibung

Hyperthyroidism

Datentyp

boolean

Alias
UMLS CUI [1]
C0020550
patients with mental illness, acrasia
Beschreibung

Mental disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C0004936
female patients in pregnancy, lactation period and planning to get pregnant during the trial
Beschreibung

Pregnancy | Breast Feeding | Pregnancy, Planned

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
any significant disorder that in the investigator's opinion, might put the patients at risk or influence the study outcomes
Beschreibung

Disorder | Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348568
acupuncture contraindications: serious allergic or infectious dermatitis and hemorrhagic diseases such as thrombocytopenic purpura and hemophilia
Beschreibung

Contraindications | Acupuncture | Dermatitis, Atopic | Infective eczematoid dermatitis | Hemorrhagic Disorders

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0683526
UMLS CUI [1,2]
C0001299
UMLS CUI [2]
C0011615
UMLS CUI [3]
C0085658
UMLS CUI [4]
C0019087
UMLS CUI [5]
C0857305
UMLS CUI [6]
C0684275
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Asthma NCT01931696

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01931696
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Mild persistent asthma | Moderate persistent asthma
Item
patients diagnosed with mild-to-moderate persistent asthma
boolean
C1960046 (UMLS CUI [1])
C1960047 (UMLS CUI [2])
Forced Expiratory Volume in 1 Second Reversibility | post bronchodilator
Item
forced expiratory volume in one second (fev1) reversibility of greater than or equal to 12% following bronchodilator administration (2 puffs)
boolean
C3830088 (UMLS CUI [1,1])
C2599594 (UMLS CUI [1,2])
Informed consent
Item
patients who have given written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
participation in another clinical trial 1 month prior to study entry
boolean
C2348568 (UMLS CUI [1])
Systemic steroids | Use of
Item
use of systemic corticosteroids 2 weeks prior to study entry
boolean
C2825233 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
Communicable Diseases | Lower respiratory tract infection | Tuberculosis, Pulmonary | Mycoses
Item
patients with general infection, lower respiratory infection, pulmonary tuberculosis and fungal infection 1 month prior to study entry
boolean
C0009450 (UMLS CUI [1])
C0149725 (UMLS CUI [2])
C0041327 (UMLS CUI [3])
C0026946 (UMLS CUI [4])
Hospitalization | exacerbation acute
Item
hospitalization due to acute exacerbation 3 months prior to study entry
boolean
C0019993 (UMLS CUI [1,1])
C0743630 (UMLS CUI [1,2])
Inhaled steroids | Theophylline | Adrenergic beta-2 Receptor Agonists | Cromolyn Sodium | Leukotriene Antagonists | Anticholinergic Agents
Item
patients cannot stop using forbidden drugs which include inhaled corticosteroid, theophylline, long-term β2 agonist, sodium cromoglicate, leukotrienes antagonist and anticholinergic drug
boolean
C2065041 (UMLS CUI [1])
C0039771 (UMLS CUI [2])
C2936789 (UMLS CUI [3])
C0012694 (UMLS CUI [4])
C0595726 (UMLS CUI [5])
C0242896 (UMLS CUI [6])
Hypersensitivity | Albuterol | Adrenal Cortex Hormones
Item
patients who are allergic to albuterol and corticosteroid
boolean
C0020517 (UMLS CUI [1,1])
C0001927 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0001617 (UMLS CUI [2,2])
Malignant Neoplasms | Cardiovascular Diseases | Liver diseases | Kidney Diseases | Hematological Disease
Item
patients with severe primary diseases such as cancer, cardiovascular system, liver, kidney and hematopoietic system diseases
boolean
C0006826 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0018939 (UMLS CUI [5])
Wheeze | Tuberculosis, Pulmonary | Bronchiectasis | Heart failure
Item
wheeze caused by pulmonary tuberculosis, bronchiectasia and cardiac insufficiency
boolean
C0035508 (UMLS CUI [1,1])
C0041327 (UMLS CUI [1,2])
C0006267 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
Hyperthyroidism
Item
patients with hyperthyroidism
boolean
C0020550 (UMLS CUI [1])
Mental disorders
Item
patients with mental illness, acrasia
boolean
C0004936 (UMLS CUI [1])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patients in pregnancy, lactation period and planning to get pregnant during the trial
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Disorder | Study Subject Participation Status
Item
any significant disorder that in the investigator's opinion, might put the patients at risk or influence the study outcomes
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
Contraindications | Acupuncture | Dermatitis, Atopic | Infective eczematoid dermatitis | Hemorrhagic Disorders
Item
acupuncture contraindications: serious allergic or infectious dermatitis and hemorrhagic diseases such as thrombocytopenic purpura and hemophilia
boolean
C0683526 (UMLS CUI [1,1])
C0001299 (UMLS CUI [1,2])
C0011615 (UMLS CUI [2])
C0085658 (UMLS CUI [3])
C0019087 (UMLS CUI [4])
C0857305 (UMLS CUI [5])
C0684275 (UMLS CUI [6])
Zum Seitenanfang zurückkehren 

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