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Recruiting NCT07439991

NCT07439991 Study of Risk Factors and Prediction of Blood Clots After Lung Cancer Surgery

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Clinical Trial Summary
NCT ID NCT07439991
Status Recruiting
Phase
Sponsor The First Hospital of Jilin University
Condition Lung Cancer (Diagnosis)
Study Type OBSERVATIONAL
Enrollment 900 participants
Start Date 2024-11-01
Primary Completion 2029-11-01

Trial Parameters

Condition Lung Cancer (Diagnosis)
Sponsor The First Hospital of Jilin University
Study Type OBSERVATIONAL
Phase N/A
Enrollment 900
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-11-01
Completion 2029-11-01
Interventions
Prospective Perioperative Data Collection

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Brief 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 Criteria

Inclusion Criteria: 1. Age ≥ 18 years 2. Patients undergoing surgical resection for lung cancer 3. Postoperative hospital stay ≥ 48 hours 4. Availability of perioperative clinical, laboratory, and imaging data 5. Willingness to provide informed consent and participate in 30-day follow-up Exclusion Criteria: 1. Pre-existing deep vein thrombosis (DVT) or pulmonary embolism (PE) before surgery 2. Preoperative or ongoing anticoagulation therapy for ≥ 2 weeks 3. Severe coagulation disorders or bleeding diseases 4. Severe hepatic, renal, or hematologic dysfunction, or uncontrolled systemic infection 5. Concurrent major organ surgery (e.g., cardiac, liver surgery) 6. Pregnancy or lactation 7. Incomplete postoperative follow-up data

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