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NCT04967651 Clinical Trial

Analysis of Risk Factors and Establishment of Early Warning Model for Pulmonary Complications

Postoperative Pulmonary Complications Clinical Trial

Official title:
Analysis of Risk Factors and Establishment and Application of a Clinical Early Warning Model for Postoperative Pulmonary Complications in Patients Undergoing Cardiac Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04967651
Other study ID # PPC202106
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 23, 2021
Est. completion date December 2022

Study information
Verified date October 2021
Source Wuhan Union Hospital, China
Contact Qingping Wu
Phone 13971605283
Email wqp1968@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Adult patients aged 18 years or older; - Elective cardiac surgery under general anesthesia Exclusion Criteria: - 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

Study Design

Related Conditions & MeSH terms

  • Postoperative Pulmonary Complications

Locations
Country Name City State
China Wuhan Union Hospital Wuhan

Sponsors (4)
Lead Sponsor Collaborator
Wuhan Union Hospital, China Qinghai People's Hospital, Shanxi cardiovascular hospital, Wuhan Central Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The occurrence of postoperative pulmonary complications 1 week after surgery
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