ID

27357

Descrição

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

Palavras-chave

  1. 09/11/2017 09/11/2017 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

9 de novembro de 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Bronchial Asthma NCT01293734

Eligibility Bronchial Asthma NCT01293734

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
age between 18 to 65 years old;
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
patients with mild-to-moderate bronchial asthma on attacking stage;
Descrição

Mild asthma Stage Progressive | Moderate asthma Stage Progressive

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0581124
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C0205329
UMLS CUI [2,1]
C0581125
UMLS CUI [2,2]
C1306673
UMLS CUI [2,3]
C0205329
without cardiopulmonary or other complications;
Descrição

Absence Complication Cardiopulmonary | Complication Absent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0009566
UMLS CUI [1,3]
C0553534
UMLS CUI [2,1]
C0009566
UMLS CUI [2,2]
C0332197
to comply with the diagnostic standard of bronchial asthma in western medicine and tcm syndrome differentiation;
Descrição

DIAGNOSTIC STANDARD Asthma | Other Coding

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0150096
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C3846158
informed consent form is required to be signed.
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
older than 65 years or younger than 18 years old;
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
pregnant woman or suckling period woman;
Descrição

Pregnancy | Breast Feeding

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients combine serious primary disease in liver, renal, cardiovascular and cerebrovascular, hemopoietic system diseases,or psychosis.
Descrição

Primary disorders Serious | Liver diseases | Kidney Diseases | Cardiovascular Diseases | Cerebrovascular Disorders | Hematological Disease | Psychotic Disorders

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0277554
UMLS CUI [1,2]
C0205404
UMLS CUI [2]
C0023895
UMLS CUI [3]
C0022658
UMLS CUI [4]
C0007222
UMLS CUI [5]
C0007820
UMLS CUI [6]
C0018939
UMLS CUI [7]
C0033975
severe levels of disease is between severe and critical extent. combine pulmonary heart disease or respiratory failure;
Descrição

Disease Severe | Critical Illness | Cor pulmonale | Respiratory Failure

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0010340
UMLS CUI [3]
C0034072
UMLS CUI [4]
C1145670
irritable the physique, or allergic to the given composition of drugs in this research;
Descrição

Physique irritable | Hypersensitivity Investigational New Drugs

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0424611
UMLS CUI [1,2]
C0436602
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0013230
patients who are in the process of other clinical research.
Descrição

Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Bronchial Asthma NCT01293734

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Informed Consent
Item
informed consent form is required to be signed.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
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])
Study Subject Participation Status
Item
patients who are in the process of other clinical research.
boolean
C2348568 (UMLS CUI [1])

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

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