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Definition of ARDS in Qinghai Province: Verification of Berlin Definition Plateau Criteria

Definition of Acute Respiratory Distress Syndrome in Plateau of Qinghai in China: Verification of Berlin Definition Plateau Criteria

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04199650
Enrollment
253
Registered
2019-12-16
Start date
2019-04-01
Completion date
2020-08-30
Last updated
2019-12-16

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

Conditions

ARDS, High Altitude

Brief summary

The severity stratification criteria for acute respiratory distress syndrome (ARDS) in Xi'ning Qinghai province (mean altitude: 2200m) were clarified according to the oxygenation index (PaO2/FiO2).

Detailed description

This study is a single-center retrospective study. According to the Berlin diagnostic standard, ARDS patients admitted to the Department of severe Medicine, affiliated Hospital of Qinghai University from January 2018 to December 2018 were divided into three groups: mild (153mmHg \< PaO2/ FiO2 ≥ 230 mmHg), moderate (76mmHg \< PaO2/ FiO2 ≥ 153 mmHg) and severe (PaO2/ FiO2 ≥ 76 mmHg). The ICU mortality, 28-day mortality, non-ventilator time in ICU, ICU hospitalization time and non-I hospitalization were observed respectively. The difference of CU time and total hospitalization days.

Interventions

None listed

Sponsors

Affiliated Hospital of Qinghai University
CollaboratorOTHER
Southeast University, China
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* 18 years of age * Meet the diagnostic criteria of ARDS * Receive invasive mechanical ventilation

Exclusion criteria

* Receive a large number of hormone shock therapy in a short period of time * Death within a short period of time (\< 24 h) after mechanical ventilation * No chest imaging data * Data missing

Design outcomes

Primary

MeasureTime frameDescription
ICU mortalityup to 24 weeksMortality during treatment in ICU
28-days mortality rate28 days after dischargeMortality at 28 days of hospitalization

Secondary

MeasureTime frameDescription
Ventilator Free timeup to 24 weeksVentilator time not used in ICU
Ventilator timeup to 24 weeksVentilator time in ICU
Hospital length of stayup to 24 weeksTotal length of stay in hospital

Countries

China

Contacts

Primary ContactGan Guifen, Bachelor
xzhd1991@163.com15897083336
Backup ContactPan Chun, Doctor
panchun1982@gmail.com13814009925

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026