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Efficacy of positive end-expiratory pressure titration after the alveolar recruitment manoeuvre in patients with acute respiratory distress syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN79027921
Enrollment
100
Registered
2008-10-31
Start date
2004-06-01
Completion date
Unknown
Last updated
2015-01-13

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 Adult respiratory distress syndrome

Interventions

Control group: The FiO2-PEEP strategy has been used in previous ARDS Network studies. PEEP and FiO2 were set according to the table of lower PEEP/higher FiO2 combinations, with the goal of obtaining

Sponsors

Asan Medical Center (South Korea)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Criteria of ARDS proposed by the American-European Consensus Conference: 1.1. Acute onset 1.2. Presence of hypoxaemia (arterial oxygen tension/fraction of inspired oxygen (FiO2) (PF ratio) less than 200 mmHg regardless of the PEEP level) 1.3. Bilateral and diffuse opacities seen on frontal chest X-ray film 1.4. Absence of left ventricular failure with pulmonary arterial occluded pressure less than 18 mmHg 2. Recruited into the trial within 48 hours of meeting above ARDS criteria 3. Aged 18 - 82 years, either sex

Exclusion criteria

Exclusion criteria: 1. Haemodynamic instability 2. Elevated intracranial pressure 3. High risk of mortality within 3 months from other than ARDS (severe organ failure, and cancer patients in terminal stages of the disease) 4. Refusal to participate

Design outcomes

Primary

MeasureTime frame
28-day mortality

Secondary

MeasureTime frame
1. Duration of mechanical ventilation 2. Intensive Care Unit (ICU) stay 3. Use of paralysing or sedative agents Measured until leaving the hospital.

Countries

Korea, South

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026