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The clinical study of the effects of prone positioning in severe respiratory distress syndrome in patients after surgical repair of acute type A aortic dissection

The clinical study of the effects of prone positioning in severe respiratory distress syndrome in patients after surgical repair of acute type A aortic dissection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052001
Enrollment
Unknown
Registered
2021-10-12
Start date
2021-10-18
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Acute respiration distress syndrome

Interventions

Experimental group:Prone ventilation

Sponsors

Xiamen Cardiovascular Hospital Affiliated to Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnose aortic dissection via aortic computed tomography angiography; 2. Aged >= 18 years old; 3. Perform surgical treatment of aortic dissection; 4. No cognitive impairment (SPMSQ = 0.6, PEEP >= 5 cmH2O) occurred.

Exclusion criteria

Exclusion criteria: 1. Patients with intracranial hypertension (ICP > 30 mmHg or cerebral perfusion pressure < 60 mmHg) or spinal cord injury and lumbar drainage; 2. Mean arterial pressure < 65 mmHg; 3. Untreated pneumothorax accompanied by chest duct leakage; 4. Have a history of mental illness; 5. Participants in other psychosocial intervention measures during the same period; 6. Pulmonary embolism; 7. Deep vein thrombosis, the course of disease is within 2 days; 8. Those who withdraw during the study period.

Design outcomes

Primary

MeasureTime frame
Mechanical ventilation duration;

Secondary

MeasureTime frame
Length of ICU(intensive care unit) hospital stay;Oxygenation index changes;

Countries

China

Contacts

Public ContactWang Juxiang

Xiamen Cardiovascular Hospital Affiliated to Xiamen University

xmwjx2012@126.com+86 15359359336

Outcome results

None listed

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