Prediction of outcome in patients with lung impairment: a prospective comparison using different scores

Prediction of outcome in patients with ARDS: a prospective comparison of ARDS-definitions and other ARDS-associated parameters, ratios and scores at intubation and over time

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

ISRCTN

Registry ID

ISRCTN32938630

Enrollment

100

Registered

2019-06-21

Start date

2015-05-28

Completion date

Unknown

Last updated

2023-08-02

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

Conditions

Acute respiratory distress syndrome (ARDS) Respiratory

Interventions

Due to the observational design of the study no specific intervention related to the study was performed. Routine data of patients with ARDS and (if available irrespectively of the study) data from Pi

PiCCO

Pulsion Medical Systems

Feldkirchen, Germany), if the PiCCO-monitoring is available irrespectively of the study. All patients received normal routine care and there was no follow-up period beyond 28-day mort

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged 18 or older 2. Critically ill 3. Acute respiratory distress syndrome (ARDS) according to Berlin Definition

Exclusion criteria

Exclusion criteria: Pregnancy

Design outcomes

Primary

Measure	Time frame
28-day mortality measured using medical records	—

Secondary

Measure	Time frame
There are no secondary outcome measures	—

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026