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Enrolling by invitation NCT06566053

Establishment of a Predictive System for Perioperative Risk Assessment and Electronic Flowcharting Response Strategies in Thoracic Surgery

Observational Perioperative Complications

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: Observation.
Who it may be relevant to
Registry conditions: Perioperative Complications. 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 →

Overview

1. To establish a risk assessment scale for thoracic surgery for the Chinese population, and to classify patients; risk according to the relevant scale; 2. Combining the guidelines for the management of acute and critical illnesses in thoracic surgical care units and the characteristics of diagnosis and treatment operations, to make an AI-assisted diagnosis and treatment process software; 3. Evaluate whether the software can provide timely and correct diagnosis and treatment recommendations for critically ill patients, shorten the time for homogenized training of specialist intensivists, and reduce the hospitalization cost of patients under the review of resident training instructors of various specialties.

Interventions

  • Other Observation
    Observation

Primary outcome measures

  • Acute Respiratory Distress Syndrome [Time frame: 2024.8-2024.12]
Secondary outcome measures (6)
  • In hospital mortality [Time frame: 2024.8-2024.12]
  • Length of hospital stay [Time frame: 2024.8-2024.12]
  • Length of ICU stay [Time frame: 2024.8-2024.12]
  • Length of postoperative stay [Time frame: 2024.8-2024.12]
  • Duration of mechanical ventilation [Time frame: 2024.8-2024.12]
  • Duration of HFNC [Time frame: 2024.8-2024.12]

Eligibility criteria

Inclusion criteria

  • Patients admitted to the Department of Thoracic Surgery of the Second Xiangya Hospital of Central South University for surgical treatment.

Exclusion criteria

  • Patients admitted to the Department of Thoracic Surgery of the Second Xiangya Hospital of Central South University without surgical treatment.

Patients under the age of 18.

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 Second Xiangya Hospital of Central South University — Changsha

Identifiers

NCT: NCT06566053 · LYF2023105

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗