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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02944279
Other study ID # 2009-1014
Secondary ID
Status Completed
Phase N/A
First received October 21, 2016
Last updated October 23, 2016
Start date January 2011
Est. completion date August 2014

Study information

Verified date October 2016
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority China: Beijing Municipal Bureau of Health
Study type Observational

Clinical Trial Summary

The acute respiratory distress syndrome (ARDS), characterized by alveolar flooding with protein-rich pulmonary edema fluid, is one of the most common disease in the intensive care unit (ICU) throughout the world. In recent years, much effort has been focused on the biological markers for their potential values to diagnose ARDS and outcomes.

ARDS is generally accompanied by the disruption in alveolar-capillary barrier permeability, which subsequently caused an influx of neutrophils into the interstitium and alveolar space. It was reported that the aggregation, adhesion activation and release proteases of neutrophils are the key pathogenesis of ARDS pulmonary edema. Neutrophil Elastase (HNE), the most crucial protease generated in neutrophil azurophilic granules, plays an important role in various inflammations, especially the lung injury. The destructive action of HNE on almost all extracellular matrix influences cell signaling through cleavage of surface receptors. Once released in circulation, HNE is rapidly inactivated by conjugation with PI3. This local inhibitor reduces HNE mediated tissue injury and inflammation. Thus, the investigators plan to conduct a cohort study with repeated measures to examine the diagnostic and prognostic value of HNE and PI3 for ARDS.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Exclusion Criteria:

- Age <18 years

- History of chronic lung diseases, such as interstitial pulmonary fibrosis or bronchiolitis

- history of pneumonectomy

- Treatment with immunomodulating therapy other than corticosteroids, such as granulocyte colony stimulating factor, cyclophosphamide, cyclosporine, interferon, or TNF-a antagonists

- Presence of other immunodeficient conditions, such as HIV infection, leukemia, or neutropenia (absolute neutrophil count <1000/µl)

- History of organs or bone marrow transplant other than autologous bone marrow transplant

- Directive to withhold intubation

- ICU stay duration<72h

- Patient developed ARDS before ICU admission. Sepsis and septic shock were defined according to the Berlin definition

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Acute Lung Injury
  • Acute Respiratory Distress Syndrome, ARDS
  • Respiratory Distress Syndrome, Adult
  • Respiratory Distress Syndrome, Newborn
  • Syndrome

Locations

Country Name City State
n/a

Sponsors (5)

Lead Sponsor Collaborator
Peking University Third Hospital Beijing Friendship Hospital, Beijing Shijitan Hospital, Beijing Xiyuan Hospital, China-Japan Friendship Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary ARDS development-Berlin definition 60 days No
Primary ARDS survival 60 days No