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Clinical Trial Summary

From January 1, 2023 to December 30, 2023, patients who were suspected of pulmonary embolism and underwent CTPA examination at Nanyang Hospital of Southern Medical University were divided into pulmonary embolism group and non pulmonary embolism group. 1. Collect relevant data, including gender, age, primary disease, CTPA imaging and reports, BNP, troponin, electrocardiogram, cardiac ultrasound, PT, APTT, TT, fibrinogen, D-dimer, etc., and analyze demographic data, pulmonary embolism risk grading, APTT/fibrinogen ratio, and determine their cut-off values through statistical analysis of the two groups. 2. Follow up on the APTT/fibrinogen ratio after anticoagulation treatment and bleeding in the pulmonary embolism group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06192199
Study type Observational
Source Nanfang Hospital, Southern Medical University
Contact Xintong Huang
Phone 8619355230761
Email 1556807596@qq.com
Status Recruiting
Phase
Start date January 1, 2024
Completion date December 1, 2026

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