The Effect of Perioperative Factors on Postoperative Outcomes After Lung Transplantation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intenvention.
- Who it may be relevant to
- Registry conditions: Postoperative Complications After Lung Transplantation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Effect of Perioperative Factors on Postoperative Outcomes in Patients Undergoing Lung Transplantation: a Prospective Observational Study
Overview
1. Evaluate the influence of perioperative factors on postoperative outcomes in patients undergoing lung transplantation patients. 2. To evaluate the feasibility of using pulmonary ultrasound to identify lung complications such as atelectasis and pulmonary edema after lung transplantation 3. Observe the changes of perioperative inflammation and immune indexes after lung transplantation
Interventions
- Other No intenvention
No intenvention
Primary outcome measures
- Postoperative pulmonary complications [Time frame: 3 days after surgery]
- Mortality [Time frame: 1 year after surgery]
Secondary outcome measures (1)
- Inflammatory index IL-6 [Time frame: 3 days after after surgery]
Eligibility criteria
Inclusion criteria
Prosedure of lung transplantation, Aged more than 18 years old
Exclusion criteria
Secondary lung transplantation, multiple organ transplantation, refusal to participate
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- Department of Anesthesiology, Second Affiliated Hospital, Zhejiang University School of Me — Hangzhou
Identifiers
NCT: NCT06603350 · 2023-0764