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Study identifier: NCT07575503 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

Diagnostic Value of Photon-Counting CT in Subsegmental Pulmonary Embolism

Condition: Subsegmental Pulmonary Embolism · Photon-Counting Computed Tomography  ·  Sponsor: Second Affiliated Hospital, Zhejiang University, School of Medicine

PhaseN/A
Planned participants696
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereHangzhou, Zhejiang, China

Interested? Contact the study team ↓

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About this study

Pulmonary embolism (PE) is a serious and potentially life-threatening condition caused by blood clots in the lungs. A particular type, subsegmental pulmonary embolism (SSPE), involves very small branches of the pulmonary arteries. Although these clots occur in smaller vessels, their risk of recurrence and complications may be similar to larger clots. Conventional CT pulmonary angiography (CTPA) is the standard imaging test for suspected PE, but image quality can sometimes be limited by motion artifacts, poor contrast filling, or body habitus, making the detection of SSPE challenging. Photon-counting computed tomography (PCCT) is a new CT technology that provides higher image resolution, lower radiation dose, and improved visualization of small blood vessels. Early studies suggest PCCT may reduce motion artifacts and increase the accuracy of detecting SSPE compared with conventional CT. This prospective cohort study will compare PCCT with dual-source CT in patients with suspected acute PE. The study aims to determine whether PCCT improves the detection rate and image quality for SSPE, and whether it can provide more reliable diagnostic information to guide clinical care.

This description comes directly from the study's public registry record.

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Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Age ≥ 18 years 2. Clinical manifestations supporting the diagnosis of acute pulmonary embolism, including: Acute onset or progressive dyspnea Unexplained hypoxemia Chest pain Hemoptysis Syncope or presyncope Combined with abnormal findings on electrocardiogram, echocardiography, or pulse oximetry 3. Revised simplified Geneva score ≥ 3 4. Written informed consent obtained from the patient or the patient's legally authorized representative Exclusion Criteria: 1. Patients requiring prophylactic or therapeutic doses of anticoagulant medication for reasons other than venous thromboembolism (VTE). 2. Life expectancy less than three months. 3. Patients unable to undergo CT scanning due to severe condition or hemodynamic instability. 4. History of allergy to contrast media, renal insufficiency (creatinine clearance \< 30 mL/min), or ongoing long-term dialysis. 5. Pregnancy. 6. Refusal to provide informed consent or inability to complete follow-up for any reason.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

The Second Affiliated Hospital of Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting

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Hangzhou

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