ID

12565

Descripción

Emergency Department (ED)-Directed Interventions to Improve Asthma Outcomes; ODM derived from: https://clinicaltrials.gov/show/NCT01079000

Link

https://clinicaltrials.gov/show/NCT01079000

Palabras clave

Versiones (1)
  1. 30/11/15 30/11/15 -
Subido en

30 de noviembre de 2015

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Acute Asthma NCT01079000

Inglés

Eligibility Acute Asthma NCT01079000

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 17-55 years old;
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients treated and discharged from one of the four study sites with acute asthma during the study period;
Descripción

(not simply for a prescription refill)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0019993
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
Descripción

patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0262926
UMLS CUI [2]
C0004096
UMLS CUI [3]
C0349790
patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
Descripción

evidence of airflow obstruction on presentation at the ed

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1527303
patients must not have a history of more than 20 pack-years of smoking;
Descripción

patients must not have a history of more than 20 pack-years of smoking

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038586
all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
Descripción

(fp, nurse practitioner or internist)

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0033131
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
Descripción

suspected copd patients and patients who require different treatments

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024117
patients with asthma who are primarily cared for by a respirologist/pulmonologist;
Descripción

patients with asthma who are primarily cared for by a respirologist/pulmonologist

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0421318
patients not seen by an emergency physician in the ed
Descripción

(e.g., direct referrals)

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2065341
physician diagnosis of acute copd
Descripción

(e.g., failure of fev1 or pef to respond to ed treatment and a fev1/fvc ratio ≤ 70%);

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0340044
radiologically confirmed pneumonia during the 10 days preceding trial entry;
Descripción

radiologically confirmed pneumonia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3843750
patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
Descripción

active history of bronchiectasis, cystic fibrosis, or lung cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006267
UMLS CUI [2]
C0010674
UMLS CUI [3]
C0242379
clinically confirmed congestive heart failure at ed presentation;
Descripción

congestive heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018802
patients not able/unwilling to perform spirometry assessment
Descripción

patients not able/unwilling to perform spirometry assessment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0037981
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
Descripción

inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
patient has previously participated in the study;
Descripción

patient has previously participated in the study;

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
patients who in the opinion of the investigator are unsuitable for enrolment.
Descripción

patients who in the opinion of the investigator are unsuitable for enrolment.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
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Similar models

Eligibility Acute Asthma NCT01079000

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 17-55 years old;
boolean
C0001779 (UMLS CUI [1])
patients treated and discharged from one of the four study sites with acute asthma during the study period;
Item
patients treated and discharged from one of the four study sites with acute asthma during the study period;
boolean
C0349790 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician
Item
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
boolean
C0262926 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
C0349790 (UMLS CUI [3])
evidence of airflow obstruction on presentation at the ed
Item
patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
boolean
C1527303 (UMLS CUI [1])
patients must not have a history of more than 20 pack-years of smoking
Item
patients must not have a history of more than 20 pack-years of smoking;
boolean
C0038586 (UMLS CUI [1])
all patients should have a Primary care physician
Item
all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
boolean
C0033131 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
suspected copd patients and patients who require different treatments
Item
these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
boolean
C0024117 (UMLS CUI [1])
patients with asthma who are primarily cared for by a respirologist/pulmonologist
Item
patients with asthma who are primarily cared for by a respirologist/pulmonologist;
boolean
C0421318 (UMLS CUI [1])
patients not seen by an emergency physician
Item
patients not seen by an emergency physician in the ed
boolean
C2065341 (UMLS CUI [1])
physician diagnosis of acute copd
Item
physician diagnosis of acute copd
boolean
C0340044 (UMLS CUI [1])
radiologically confirmed pneumonia
Item
radiologically confirmed pneumonia during the 10 days preceding trial entry;
boolean
C3843750 (UMLS CUI [1])
active history of bronchiectasis, cystic fibrosis, or lung cancer
Item
patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
boolean
C0006267 (UMLS CUI [1])
C0010674 (UMLS CUI [2])
C0242379 (UMLS CUI [3])
congestive heart failure
Item
clinically confirmed congestive heart failure at ed presentation;
boolean
C0018802 (UMLS CUI [1])
patients not able/unwilling to perform spirometry assessment
Item
patients not able/unwilling to perform spirometry assessment
boolean
C1321605 (UMLS CUI [1])
C0037981 (UMLS CUI [2])
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
Item
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
boolean
C0021430 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
patient has previously participated in the study;
Item
patient has previously participated in the study;
boolean
C2348568 (UMLS CUI [1])
patients who in the opinion of the investigator are unsuitable for enrolment.
Item
patients who in the opinion of the investigator are unsuitable for enrolment.
boolean
C1321605 (UMLS CUI [1])
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