ID

14139

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01931696

Nyckelord

  1. 2016-03-31 2016-03-31 -
Uppladdad den

31 mars 2016

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Asthma NCT01931696

Eligibility Asthma NCT01931696

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01931696
Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Mild persistent asthma | Moderate persistent asthma

Datatyp

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)
Beskrivning

Forced Expiratory Volume in 1 Second Reversibility | post bronchodilator

Datatyp

boolean

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

Informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

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

Study Subject Participation Status

Datatyp

boolean

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

Systemic steroids | Use of

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

Hospitalization | exacerbation acute

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

Hypersensitivity | Albuterol | Adrenal Cortex Hormones

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

Wheeze | Tuberculosis, Pulmonary | Bronchiectasis | Heart failure

Datatyp

boolean

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

Hyperthyroidism

Datatyp

boolean

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

Mental disorders

Datatyp

boolean

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

Pregnancy | Breast Feeding | Pregnancy, Planned

Datatyp

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
Beskrivning

Disorder | Study Subject Participation Status

Datatyp

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
Beskrivning

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

Datatyp

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

Similar models

Eligibility Asthma NCT01931696

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01931696
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial