Skip to content

Effect of sequential lateral positioning in mechanically ventilated patients with stroke-related pneumonia

Effect of sequential lateral positioning in mechanically ventilated patients with stroke-related pneumonia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100089
Enrollment
Unknown
Registered
2025-04-02
Start date
2025-04-07
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Stroke-related pneumonia

Interventions

Experimental group:The patients will be placed in 5 positions in the order of 5 positions with usual care and sequential lateral positioning, and each position will be held for 30 minutes.
Control group:The patient will be turned over and given back percussion every 2 hours with usual care and positioning, and reincubated for 2 hours to change direction.

Sponsors

The First Affiliated Hospital of NanChang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for stroke and be confirmed by head CT scan or MRI; (2) meet the latest diagnostic criteria for stroke-related pneumonia; (3) Age >= 18 years old; (4) Body mass index <= 35kg/m^2; (5) invasive mechanical ventilation is required; (6) The patient or family agrees to participate in the study

Exclusion criteria

Exclusion criteria: (1) Mechanical ventilation time= 48 hours (including discharge and clinical death); (2) multi-organ failure; (3) Haemodynamically unstable patients: adequate fluid resuscitation and two vasopressors in the past 6 hours, or a 30% increase in vasopressor dose, but a sustained mean arterial pressure of less than 60mmHg; (4) Exclude contraindications to lateral decubitus ventilation caused by traumatic factors such as pulmonary contusion, lung infection, respiratory failure, multiple fractures or rib fractures that lead to inability to lie on the side, or severe pressure injury on one side, pleural effusion, etc.; (5) Obvious abdominal distention, gastric residual > 400ml; (6) pneumothorax; (7) Increased intracranial pressure.

Design outcomes

Primary

MeasureTime frame
PaO2/FiO2 ratio;inflammatory markers;

Secondary

MeasureTime frame
24-hour airway sputum aspiration;Duration of mechanical ventilation;

Countries

China

Contacts

Public ContactWang dan

The First Affiliated Hospital of NanChang University

1464766089@qq.com+86 139 7911 9716

Outcome results

None listed

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