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Standard Treatment Compliance of Participants, Effectiveness and Prognosis in Acute Respiratory Distress Syndrome

Standard Treatment Compliance of Participants, Effectiveness and Prognosis in Acute Respiratory Distress Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02178982
Acronym
APT
Enrollment
134
Registered
2014-07-01
Start date
2014-05-31
Completion date
2015-06-30
Last updated
2015-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome, Respiratory Failure

Keywords

mechanical ventilation, ARDS, Ventilator strategy, outcome

Brief summary

The Acute Respiratory Distress Syndrome (ARDS) is one of common clinical critically diseases. In the United States, the incidence of ARDS reaches 31%, which is one of the main causes of death in patients. There is no unified treatment process for ARDS currently and the treatment measures are not yet standardized, so the standardization of ARDS treatment processes is needed to reduce mortality in patients. Following the evidence-based medicine principles and six-step treatment standards of ARDS, this study uses the method of multi-center randomized controlled clinical trials to evaluate the standardized treatment process of ARDS, which provides the basis for the standardized treatment of ARDS.

Interventions

None listed

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* aged ≥ 18 years * admitted to the ICU * according to the diagnostic criteria of ARDS Berlin definition,admit patients with severe ARDS

Exclusion criteria

* age \<18 years old * be expected to die within 24 hours * end-stage malignancies * be participating in other studies, which may affect the results of this study * DNI (do not intubation) and DNR (do not recovery) patients * family members do not agree to sign an informed consent

Design outcomes

Primary

MeasureTime frame
Number of medical staff who comply the protocol treatment2 years

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026