- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02490215
Epidemiology of Acute Respiratory Distress Syndrome in Chinese ICUs
Studieoversikt
Status
Forhold
Detaljert beskrivelse
All patients admitted to the participating ICUs during a 6-month period(from January 1, 2015 to July 1,2015 ) will be screened at ICU admission and daily for the occurrence of ARDS ( AECC criteria) for a maximum of 28 days after ICU admission.
Data collection:
- For all patients, Demographic characteristics, admission category, the patient source intervention during ICU , APACHEII , SOFA score and discharge information will be collected
- For patients with ARDS, data about ABG , parameters of MV, hemodynamic on day0 to day7 and last day of MV will be collected.
- For patients without ARDS at ICU admission, data about risk factor for ARDS ,such as LIPS score, parameters of MV , and fluid balance on ICU day0 to day7 will be collected.
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
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Beijing
-
Beijing, Beijing, Kina
- Peking University People's Hospital
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Beijing, Beijing, Kina, 100730
- MICU, Peking union medical college hospital
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Beijing, Beijing, Kina
- Beijing Hospital of Ministry of Health
-
Beijing, Beijing, Kina
- Department of Critical Care Medicine, Fuxing Hospital, Capital Medical University
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Beijing, Beijing, Kina
- General ICU, Beijing Tongren Hospital, Capital Medical University
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Beijng, Beijing, Kina
- China-Japan Friendship Hospital
-
-
Chongqing
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ChongQing, Chongqing, Kina
- Department of Emergency and Intensive Care Medicine, The First Affiliated Hospital of Chongqing Medical University
-
-
Fujian
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Fuzhou, Fujian, Kina
- The First Affiliated Hospital of Fujian Medical University
-
-
Guangdong
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Guangzhou, Guangdong, Kina
- Department of CriticalCare Medicine, Guangdong General Hospital
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-
Hainan
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HaiKou, Hainan, Kina
- Department of Critical Care Medicine, Hainan Provincial People's Hospital
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-
Hebei
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Shijiazhuang, Hebei, Kina
- Department of Critical Care Medicine, Hebei Medical University Fourth Hospital
-
-
Heilongjiang
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Harbin, Heilongjiang, Kina
- Department of Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University
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Henan
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Zhengzhou, Henan, Kina
- ICU, The First Affiliated Hospital, Zhengzhou University
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Hubei
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WuHan, Hubei, Kina
- Department of Critical Care Medicine, Tongji Hospital of Tongji Medical College, Huazhong University of Science & Technology
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Hunan
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Changsha, Hunan, Kina
- Department of Critical Care Medicine, Xiangya Hospital, Central South University
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Inner Mongolia
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Hohhot, Inner Mongolia, Kina
- Department of Critical Care Medicine, The Affiliated Hopsital of Inner Mongolia Medical University
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Jilin
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ChangChun, Jilin, Kina
- Department of Critical Care Medicine, The Second Hospital of Jilin University
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Liaoning
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Shenyang, Liaoning, Kina
- Department of Critical Care Medicine, The First Affiliated Hospital of China Medical University
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Ningxia
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YinChuan, Ningxia, Kina
- General Hospital of Ningxia Medical University
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Shandong
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Jinan, Shandong, Kina
- Department of Critical Care Medicine, Qilu Hospital of Shandong University
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Shanghai
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Shanghai, Shanghai, Kina
- Emergency ICU, Ruijin Hospital, Shanghai Jiao Tong University
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Shanxi
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XiAn, Shanxi, Kina
- Surgical Intensive Care Unit, Xijing Hospital
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Sichuan
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Chengdu, Sichuan, Kina
- Department of Critical Care Medicine, West China Hospital, Sichuan University
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Xinjiang
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Urumqi, Xinjiang, Kina
- Department of Critical Care Medicine, First Affiliated Hospital, Xinjiang Medical University
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Yunnan
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Kunming, Yunnan, Kina
- Department of Emergency Medicine and Medical ICU, The First Affiliated Hospital of Kunming Medical University
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Zhejiang
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Hangzhou, Zhejiang, Kina
- Department of Critical Care Medicine, Zhejiang Provincial People's Hospital
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
all patients age >18 yrs admitted to 24 participating ICUs
Exclusion Criteria:
No patients should be excluded (regardless of age, underlying disease, life expectancy, etc).
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
|
ARDS, non-ARDS
patients with ARDS and patients without ARDS
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
incidence of acute respiratory distress syndrome (ARDS)
Tidsramme: from ICU admission to 28-day of ICU stay
|
incidence of ARDS = the number of patients developing ARDS during ICU / the total number of patients admitted to ICU
|
from ICU admission to 28-day of ICU stay
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
ICU mortality of patients with ARDS
Tidsramme: followed up to 3 months after inclusion or to ICU discharge, whichever occurred first
|
followed up to 3 months after inclusion or to ICU discharge, whichever occurred first
|
|
hospital mortality of patients with ARDS
Tidsramme: followed up to 3 months after inclusion or to hospital discharge, whichever occurred first
|
followed up to 3 months after inclusion or to hospital discharge, whichever occurred first
|
Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: Bin Du, MICU of Peking Union Medical College Hospital
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- MICU2015_1
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