ID

31550

Beschrijving

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

Trefwoorden

Versies (1)
  1. 03-09-18 03-09-18 -
Houder van rechten

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

Geüploaded op

3 september 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Cough Variant Asthma NCT01170429

Engels

Eligibility Cough Variant Asthma NCT01170429

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Gender and Age

Datatype

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;
Beschrijving

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

Datatype

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;
Beschrijving

Without wheeze and fever

Datatype

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;
Beschrijving

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

Datatype

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;
Beschrijving

Without rales from lung

Datatype

boolean

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

No obvious abnormalities from chest x-ray

Datatype

boolean

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

Positive bronchial provocation test

Datatype

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with chronic pulmonary disease;
Beschrijving

Chronic pulmonary disease

Datatype

boolean

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

Allergy to ß2 receptor agonist

Datatype

boolean

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

Long-term treatment with ß2 receptor agonist

Datatype

boolean

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

Severe heart, renal and hepatic disease

Datatype

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;
Beschrijving

Non-compliance

Datatype

boolean

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

Pregnancy, breast feeding and childbearing potential women

Datatype

boolean

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

Ineligibility according to the investigators' judgement

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512714
UMLS CUI [1,2]
C0022423
UMLS CUI [1,3]
C0008961
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Similar models

Eligibility Cough Variant Asthma NCT01170429

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
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