NCT02174081

Brief Summary

ARDS is a severe disease, it's important to predict the incidence of ARDS.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
698

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2014

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2014

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 11, 2014

Completed
14 days until next milestone

First Posted

Study publicly available on registry

June 25, 2014

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
Last Updated

June 28, 2016

Status Verified

June 1, 2016

Enrollment Period

2 years

First QC Date

June 11, 2014

Last Update Submit

June 27, 2016

Conditions

ARDSSeptic Shock

Keywords

mechanical ventilation, ARDS, Ventilator strategy, outcome

Outcome Measures

Primary Outcomes (1)

  • incidence of ARDS

    evaluate the incidence of risk factors of ARDS

    up to 24 months

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients have the risk of ARDS

You may qualify if:

  • Critically ill patients who admitted into participating ICU

You may not qualify if:

  • Patients with chronic pulmonary disease such as chronic obstructive pulmonary disease (COPD), asthma, lung cancer, pulmonary fibrosis and tuberculosis Age less than 18 years old Pregnancy Died within 24 hours from ICU admission ARDS patients who diagnosed 24hours before ICU admission Referral from other hospital to participating ICU Lack of data of ARDS risk factors

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongda Hospital

Nanjing, Jiangsu, 210009, China

Location

MeSH Terms

Conditions

Shock, Septic

Condition Hierarchy (Ancestors)

SepsisInfectionsSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and SymptomsShock

Study Officials

  • Jianfeng Xie, Dr

    Southeast University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Zhongda Hospital

Study Record Dates

First Submitted

June 11, 2014

First Posted

June 25, 2014

Study Start

March 1, 2014

Primary Completion

March 1, 2016

Study Completion

June 1, 2016

Last Updated

June 28, 2016

Record last verified: 2016-06

Locations

CN(1)