ID

31550

Description

Efficacy and Safety Study of Procaterol Hydrochloride to Treat Patients With Cough Variant Asthma (CVA); ODM derived from: https://clinicaltrials.gov/show/NCT01170429 Sponsor: Shanghai Jiao Tong University School of Medicine Information provided by: Shanghai Jiao Tong University School of Medicine Principal Investigator: Xin Zhou, MD Shanghai Jiao Tong University School of Medicine

Link

https://clinicaltrials.gov/show/NCT01170429

Keywords

Versions (1)
  1. 9/3/18 9/3/18 -
Copyright Holder

Xin Zhou/Director of Respiratory Department, Shanghai Jiao Tong University Affiliated 1st People's Hospital

Uploaded on

September 3, 2018

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Cough Variant Asthma NCT01170429

English

Eligibility Cough Variant Asthma NCT01170429

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female patients,18-75 years old;
Description

Gender and Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
cough lasting over 3 weeks ; dry cough or with slight white mucous phlegm; cough is the main clinical symptom or the only symptom;
Description

Dry cough lasting over 3 weeks; cough is the main clinical symptom

Data type

boolean

Alias
UMLS CUI [1,1]
C0010200
UMLS CUI [1,2]
C0580798
UMLS CUI [2]
C0850149
UMLS CUI [3,1]
C0750482
UMLS CUI [3,2]
C1997237
UMLS CUI [4,1]
C0010200
UMLS CUI [4,2]
C3177142
without wheeze and fever;
Description

Without wheeze and fever

Data type

boolean

Alias
UMLS CUI [1,1]
C0043144
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0015967
UMLS CUI [2,2]
C0332197
without the history of upper respiratory tract infection within recent two months; non-smoking or giving-up smoking for over two years;
Description

No recent upper respiratory tract infection; non-smoking or former smoker

Data type

boolean

Alias
UMLS CUI [1,1]
C0332185
UMLS CUI [1,2]
C0041912
UMLS CUI [1,3]
C0332197
UMLS CUI [2]
C1519386
without rales from lung;
Description

Without rales from lung

Data type

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0034642
no obvious abnormalities from chest x-ray;
Description

No obvious abnormalities from chest x-ray

Data type

boolean

Alias
UMLS CUI [1,1]
C0039985
UMLS CUI [1,2]
C0205307
bronchial provocation test: positive.
Description

Positive bronchial provocation test

Data type

boolean

Alias
UMLS CUI [1,1]
C0006265
UMLS CUI [1,2]
C1446409
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with chronic pulmonary disease;
Description

Chronic pulmonary disease

Data type

boolean

Alias
UMLS CUI [1]
C0746102
patients who are allergic to ß2 receptor agonist;
Description

Allergy to ß2 receptor agonist

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1373132
patients taking ß2 receptor agonist for long time;
Description

Long-term treatment with ß2 receptor agonist

Data type

boolean

Alias
UMLS CUI [1,1]
C2936789
UMLS CUI [1,2]
C0420257
severe heart, renal and hepatic disease;
Description

Severe heart, renal and hepatic disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0022658
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0023895
UMLS CUI [3,2]
C0205082
unable to comply with the protocol;
Description

Non-compliance

Data type

boolean

Alias
UMLS CUI [1]
C0457432
pregnant, breast feeding, and childbearing potential women;
Description

Pregnancy, breast feeding and childbearing potential women

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C3831118
patients improper to the trial according to the investigators' judgement.
Description

Ineligibility according to the investigators' judgement

Data type

boolean

Alias
UMLS CUI [1,1]
C1512714
UMLS CUI [1,2]
C0022423
UMLS CUI [1,3]
C0008961
Back to the top of the page

Similar models

Eligibility Cough Variant Asthma NCT01170429

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender and Age
Item
male or female patients,18-75 years old;
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Dry cough lasting over 3 weeks; cough is the main clinical symptom
Item
cough lasting over 3 weeks ; dry cough or with slight white mucous phlegm; cough is the main clinical symptom or the only symptom;
boolean
C0010200 (UMLS CUI [1,1])
C0580798 (UMLS CUI [1,2])
C0850149 (UMLS CUI [2])
C0750482 (UMLS CUI [3,1])
C1997237 (UMLS CUI [3,2])
C0010200 (UMLS CUI [4,1])
C3177142 (UMLS CUI [4,2])
Without wheeze and fever
Item
without wheeze and fever;
boolean
C0043144 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0015967 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
No recent upper respiratory tract infection; non-smoking or former smoker
Item
without the history of upper respiratory tract infection within recent two months; non-smoking or giving-up smoking for over two years;
boolean
C0332185 (UMLS CUI [1,1])
C0041912 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1519386 (UMLS CUI [2])
Without rales from lung
Item
without rales from lung;
boolean
C0332197 (UMLS CUI [1,1])
C0034642 (UMLS CUI [1,2])
No obvious abnormalities from chest x-ray
Item
no obvious abnormalities from chest x-ray;
boolean
C0039985 (UMLS CUI [1,1])
C0205307 (UMLS CUI [1,2])
Positive bronchial provocation test
Item
bronchial provocation test: positive.
boolean
C0006265 (UMLS CUI [1,1])
C1446409 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Chronic pulmonary disease
Item
patients with chronic pulmonary disease;
boolean
C0746102 (UMLS CUI [1])
Allergy to ß2 receptor agonist
Item
patients who are allergic to ß2 receptor agonist;
boolean
C0020517 (UMLS CUI [1,1])
C1373132 (UMLS CUI [1,2])
Long-term treatment with ß2 receptor agonist
Item
patients taking ß2 receptor agonist for long time;
boolean
C2936789 (UMLS CUI [1,1])
C0420257 (UMLS CUI [1,2])
Severe heart, renal and hepatic disease
Item
severe heart, renal and hepatic disease;
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
Non-compliance
Item
unable to comply with the protocol;
boolean
C0457432 (UMLS CUI [1])
Pregnancy, breast feeding and childbearing potential women
Item
pregnant, breast feeding, and childbearing potential women;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3])
Ineligibility according to the investigators' judgement
Item
patients improper to the trial according to the investigators' judgement.
boolean
C1512714 (UMLS CUI [1,1])
C0022423 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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