Skip to content

Acute lung injury after liver transplantation

Acute lung injury after liver transplantation

Status
Recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400085991
Enrollment
Unknown
Registered
2024-06-22
Start date
2024-06-22
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Acute lung injury

Interventions

1. Acute lung injury group :not applicable,no intervention
2. Non-acute lung injury group:not applicable,no intervention

Sponsors

Guangxi Zhuang Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Adult patients: Because the physiological structure and disease characteristics of adults are different from those of children, the study mainly included adult liver transplant patients. Clear history of liver transplantation: Patients should have a clear history of liver transplantation and have symptoms and signs of acute lung injury after surgery. Complete medical records: Patients should have complete medical records before, during and after surgery in order to accurately analyze and evaluate their condition. Informed consent: Patients or their family members need to sign an informed consent form to agree to participate in the study and understand the purpose, methods and possible risks of the study.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: Pediatric patients: Pediatric liver transplant patients were excluded from the study due to the different physiological characteristics and drug responses of children compared to adults. Other serious complications: If the patient has other serious complications or comorbidities in addition to acute lung injury, which may affect the results of the study or increase the risk of the study, it should be excluded. Incomplete medical records: If the patient's medical records are incomplete or missing key information that makes it impossible to accurately assess the patient's condition, they should be excluded from the study. Known preoperative pulmonary function abnormalities: Patients with preoperative lung function abnormalities should be excluded because it is impossible to accurately determine whether acute lung injury is caused by liver transplantation.

Design outcomes

Primary

MeasureTime frame
CXCL3;

Secondary

MeasureTime frame
Differences in the expression of inflammatory mediators;

Countries

CHINA

Contacts

Public ContactGuiting Yang

Guangxi Zhuang Autonomous Region People's Hospital

1083578014@qq.com+86 136 5771 9764

Outcome results

None listed

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