Analysis of Risk Factors and Establishment of Early Warning Model for Pulmonary Complications
1 other identifier
observational
1,000
1 country
1
Brief Summary
The purpose of this study is to collect perioperative diagnosis and treatment information for cardiac surgery patients, collect blood samples for laboratory testing when necessary, and analyze the data to clarify the risk factors of pulmonary complications in patients undergoing cardiac surgery during the perioperative period. On this basis, a clinical early warning model for pulmonary complications after cardiac surgery will be developed to reduce the risk of pulmonary complications and even death in clinical practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 15, 2021
CompletedFirst Posted
Study publicly available on registry
July 19, 2021
CompletedStudy Start
First participant enrolled
August 23, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2022
CompletedNovember 3, 2021
October 1, 2021
1.3 years
July 15, 2021
October 26, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
The occurrence of postoperative pulmonary complications
1 week after surgery
Study Arms (2)
Patients with pulmonary complications following cardiac surgery
Patients without pulmonary complications following cardiac surgery
Eligibility Criteria
Patients aged 18 years or older who planned elective cardiac surgery under general anesthesia
You may qualify if:
- Adult patients aged 18 years or older;
- Elective cardiac surgery under general anesthesia
You may not qualify if:
- Patients and their family members refused to be enrolled;
- Patients unable to communicate due to language barriers such as dementia;
- Patients admitted to ICU 24h before surgery;
- Estimated duration of surgery less than 2 hours;
- Patients died or discharged within 24 hours after surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Wuhan Union Hospital
Wuhan, China
Biospecimen
plasma
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 15, 2021
First Posted
July 19, 2021
Study Start
August 23, 2021
Primary Completion
December 1, 2022
Study Completion
December 1, 2022
Last Updated
November 3, 2021
Record last verified: 2021-10