PRone positioN in patients with spontanEous ventiLation and acute hypoxemic respIratory FailurE- The PRONELIFE Randomized Controlled Trial

PRone positioN in patients with spontanEous ventiLation and acute hypoxemic respIratory FailurE- The PRONELIFE Randomized Controlled Trial - ProneLife

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON51294

Enrollment

Registered

2022-09-16

Start date

2022-04-01

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

buikligging ter voorkoming van beademing oxygen ventilation

Interventions

prone position

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 18 year and older acute respiratory failure

Exclusion criteria

Exclusion criteria: no informed consent prone position impossible

Design outcomes

Primary

Measure	Time frame
The primary endpoint is the number of ventilator-free days at 14 days.	—

Secondary

Measure	Time frame
Secondary endpoints include the effects of prone position upon oxygenation, dyspnea, weaning from a respiratory support device, ICU and hospital length of stay, and mortality at days 28 and 90.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)