Treatment in Patients Hospitalized With Acute Exacerbation of Chronic Obstructive Pulmonary Disease (TripAE)
15. august 2014 opdateret af: Wang Ying, Beijing Chao Yang Hospital
Chronic obstructive pulmonary disease has become a serious global health care and public health problems due to its high prevalence, high morbidity and heavy economic burden.
Acute exacerbation of chronic obstructive pulmonary disease is one of the most important causes of death in patients with COPD.
Systemic corticosteroids therapy is recommended in COPD exacerbations.
In clinical practice for the treatment of acute exacerbation of COPD， antibiotic application is still controversial.
Evidence from current guideline is based on strict criteria from randomized controlled trials, thus the given condition is simplified.
Patients meet the criteria account for the minority in the real world.
Therefore, it is still not clear whether most patients benefit from the recommended treatment.
In our design, hospitalized patients with acute exacerbation of COPD will be enrolled, with their treatment, arterial hypoxemia, recovery time and length of hospitalization being observed.
The main purpose is to evaluate the benefit effect of current recommended treatment of acute exacerbation of COPD in the real world.
Studieoversigt
Status
Ukendt
Betingelser
Detaljeret beskrivelse
Chronic obstructive pulmonary disease has become a serious global health care and public health problems due to its high prevalence, high morbidity and heavy economic burden.
Acute exacerbation of COPD is one of the most important causes of death in patients with COPD.
The global strategy for the diagnosis, management, and prevention of COPD recommends systemic corticosteroids therapy in COPD exacerbations as it can shorten recovery time, reduce treatment failure, improve lung function and arterial hypoxemia.
In clinical practice for the treatment of acute exacerbation of COPD， antibiotic application is still controversial.
Evidence from current guideline is based on strict criteria from randomized controlled trials, thus the given condition is simplified.
Patients meet the criteria account for the minority in the real world.
Therefore, it is still not clear whether most patients benefit from the recommended treatment.
In our design, hospitalized patients with acute exacerbation of COPD will be enrolled, with their treatment, arterial hypoxemia, recovery time and length of hospitalization being observed.
The main purpose is to evaluate the benefit effect of current recommended treatment of acute exacerbation of COPD in the real world.
Undersøgelsestype
Observationel
Tilmelding (Forventet)
400
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
40 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Patients hospitalized with acute exacerbation of chronic obstructive pulmonary disease from 1st July, 2014 from Beijing Chao Yang Hospital
Beskrivelse
Inclusion Criteria:
- Hospitalized patients with acute exacerbation of chronic obstructive pulmonary disease
- Age≥ 40years old
Exclusion Criteria:
- The first diagnosis which caused hospitalization is not acute exacerbation of chronic obstructive pulmonary disease
- Chest radiography shows congestive heart failure
- Chest CT shows lung cancer, active pulmonary tuberculosis, pulmonary thromboembolism or interstitial lung diseases
- Serious cardiac failure, renal insufficiency or hepatic dysfunction
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
change of the score of COPD Assesment Test as a measurement of the overall condition of the patient
Tidsramme: baseline, 1 month after dischahge, 2 months after discharge
|
baseline, 1 month after dischahge, 2 months after discharge
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
change of the score of modified Medical British Research Council questionaire as a measurement of the overall condition of the patient
Tidsramme: baseline, 1 month after discharge, 2 months after discharge
|
baseline, 1 month after discharge, 2 months after discharge
|
Andre resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
percentage of use of systemic corticosteroid in patients
Tidsramme: 8 months after the first enrollment
|
8 months after the first enrollment
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Wang Ying, Master, Beijing Chao Yang Hospital
- Studiestol: Huang Kewu, M.D., Beijing Chao Yang Hospital
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. august 2014
Primær færdiggørelse (Forventet)
1. juni 2015
Studieafslutning (Forventet)
1. september 2015
Datoer for studieregistrering
Først indsendt
9. juli 2014
Først indsendt, der opfyldte QC-kriterier
15. august 2014
Først opslået (Skøn)
18. august 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
18. august 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. august 2014
Sidst verificeret
1. august 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2014-K-115
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .