Informatie:
Fout:
ID
27357
Beschrijving
Research on Traditional Chinese Medicine (TCM) Clinical Treatment of the Acute Episode of Bronchial Asthma.; ODM derived from: https://clinicaltrials.gov/show/NCT01293734
Link
https://clinicaltrials.gov/show/NCT01293734
Trefwoorden
Versies (1)
- 09-11-17 09-11-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
9 november 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Bronchial Asthma NCT01293734
Eligibility Bronchial Asthma NCT01293734
- StudyEvent: Eligibility
Similar models
Eligibility Bronchial Asthma NCT01293734
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
age between 18 to 65 years old;
boolean
C0001779 (UMLS CUI [1])
Mild asthma Stage Progressive | Moderate asthma Stage Progressive
Item
patients with mild-to-moderate bronchial asthma on attacking stage;
boolean
C0581124 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0205329 (UMLS CUI [1,3])
C0581125 (UMLS CUI [2,1])
C1306673 (UMLS CUI [2,2])
C0205329 (UMLS CUI [2,3])
C1306673 (UMLS CUI [1,2])
C0205329 (UMLS CUI [1,3])
C0581125 (UMLS CUI [2,1])
C1306673 (UMLS CUI [2,2])
C0205329 (UMLS CUI [2,3])
Absence Complication Cardiopulmonary | Complication Absent
Item
without cardiopulmonary or other complications;
boolean
C0332197 (UMLS CUI [1,1])
C0009566 (UMLS CUI [1,2])
C0553534 (UMLS CUI [1,3])
C0009566 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0009566 (UMLS CUI [1,2])
C0553534 (UMLS CUI [1,3])
C0009566 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
DIAGNOSTIC STANDARD Asthma | Other Coding
Item
to comply with the diagnostic standard of bronchial asthma in western medicine and tcm syndrome differentiation;
boolean
C0150096 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
C0004096 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
Informed Consent
Item
informed consent form is required to be signed.
boolean
C0021430 (UMLS CUI [1])
Age
Item
older than 65 years or younger than 18 years old;
boolean
C0001779 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant woman or suckling period woman;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Primary disorders Serious | Liver diseases | Kidney Diseases | Cardiovascular Diseases | Cerebrovascular Disorders | Hematological Disease | Psychotic Disorders
Item
patients combine serious primary disease in liver, renal, cardiovascular and cerebrovascular, hemopoietic system diseases,or psychosis.
boolean
C0277554 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0007222 (UMLS CUI [4])
C0007820 (UMLS CUI [5])
C0018939 (UMLS CUI [6])
C0033975 (UMLS CUI [7])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0007222 (UMLS CUI [4])
C0007820 (UMLS CUI [5])
C0018939 (UMLS CUI [6])
C0033975 (UMLS CUI [7])
Disease Severe | Critical Illness | Cor pulmonale | Respiratory Failure
Item
severe levels of disease is between severe and critical extent. combine pulmonary heart disease or respiratory failure;
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0010340 (UMLS CUI [2])
C0034072 (UMLS CUI [3])
C1145670 (UMLS CUI [4])
C0205082 (UMLS CUI [1,2])
C0010340 (UMLS CUI [2])
C0034072 (UMLS CUI [3])
C1145670 (UMLS CUI [4])
Physique irritable | Hypersensitivity Investigational New Drugs
Item
irritable the physique, or allergic to the given composition of drugs in this research;
boolean
C0424611 (UMLS CUI [1,1])
C0436602 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0436602 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Study Subject Participation Status
Item
patients who are in the process of other clinical research.
boolean
C2348568 (UMLS CUI [1])