Deep Vein Thrombosis Clinical Trials

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Prospective Cohort Study on Risk Factors and Machine Learning-Based Prediction of Postoperative Venous Thromboembolism in Patients Undergoing Lung Cancer Surgery

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about the risk factors and prediction of postoperative venous thromboembolism (VTE) in patients undergoing lung cancer surgery. The main question it aims to answer is: Which clinical, surgical, and laboratory factors are associated with the development of postoperative deep vein thrombosis (DVT) in lung cancer surgery patients, and can machine learning models accurately predict individual risk? Participants undergoing lung cancer surgery will be prospectively followed for 30 days after surgery. Perioperative clinical data, laboratory results, and imaging findings will be collected to identify VTE risk factors and to develop a predictive model.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• Patients undergoing surgical resection for lung cancer

• Postoperative hospital stay ≥ 48 hours

• Availability of perioperative clinical, laboratory, and imaging data

• Willingness to provide informed consent and participate in 30-day follow-up

Locations
Other Locations
China
The First Hospital of Jilin University, Department of Thoracic Surgery
RECRUITING
Changchun
Contact Information
Primary
Wei Liu
l_w01@jlu.edu.cn
86-13596083366
Time Frame
Start Date: 2024-11-01
Estimated Completion Date: 2029-11-30
Participants
Target number of participants: 900
Treatments
VTE Group
Adult patients undergoing lung cancer surgery who develop postoperative deep vein thrombosis (DVT) within 30 days. Perioperative clinical, laboratory, and imaging data will be collected to identify risk factors and build predictive models.
Non-VTE Group
Adult patients undergoing lung cancer surgery who do not develop postoperative DVT within 30 days. Perioperative clinical, laboratory, and imaging data will be collected for comparison with the VTE group.
Sponsors
Leads: The First Hospital of Jilin University

This content was sourced from clinicaltrials.gov