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Not yet recruiting NCT06922916

Perioperative Risk Factors Related to the Prognosis of Lung Transplantation: A Retrospective Study

— Observational COPD Interstitial Pneumonia Bronchiectasis Respiratory Failure

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: COPD, Interstitial Pneumonia, Bronchiectasis, Respiratory Failure. 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 →

Overview

This study analyzes patients who underwent lung transplantation at the First Affiliated Hospital of Zhejiang University from 2017 to 2024, focusing on anesthesia's impact on post-op results. It gathers patient data from hospital and Mediston systems, with main focus on in-hospital complications and secondary focus on ICU stay, post-op hospitalization, mortality, and intubation time. The research aims to deepen understanding of anesthetic management's role in lung transplant outcomes and guide improvements in perioperative anesthesia protocols.

Primary outcome measures

  • In-hospital adverse events [Time frame: Collect data for an expected average about 2 hours]
Secondary outcome measures (6)
  • ICU stay [Time frame: Collect data for an expected average about 2 hours]
  • Postoperative hospital stay [Time frame: Collect data for an expected average about 2 hours]
  • In-hospital mortality [Time frame: Collect data for an expected average about 2 hours]
  • 30-day postoperative mortality [Time frame: Collect data for an expected average about 2 hours]
  • 90-day postoperative mortality [Time frame: Collect data for an expected average about 2 hours]
  • The duration of endotracheal intubation [Time frame: Collect data for an expected average about 2 hours]

Eligibility criteria

Inclusion criteria

  • Age >18 years at time of transplantation
  • Received single or bilateral lung transplantation

Exclusion criteria

  • Re-transplantation
  • Multi-organ transplantation
  • Autotransplantation
  • Incomplete medical records: Recipients with >20% missing essential data elements in any of these categories:Preoperative baseline characteristics； Intraoperative parameters；Postoperative outcome measures

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
  • The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang — Hangzhou

Identifiers

NCT: NCT06922916 · ZJU2025B0268

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗