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Recruiting Not applicable

Residual Pulmonary Vascular Obstruction Index Computed With Ventilation/Perfusion SPECT/CT Imaging to Predict the Risk of Venous Thromboembolism Recurrence in Patients With Pulmonary Embolism (PRONOSPECT)

NCT06372730 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-06-11
Last updated
2026-06-15

Condition(s) studied

Pulmonary EmbolismVenous Thromboembolism

Investigational drug(s) / intervention(s)

Ventilation/Perfusion Single Photon Emission Computed Tomography (V/Q SPECT/CT)

Ventilation/Perfusion Single Photon Emission Computed Tomography (V/Q SPECT/CT): All patients will undergo a V/Q SPECT/CT scan at inclusion.

Study summary

Major risk after pulmonary embolism (PE) is recurrence, fatal in 10% of patients. Patients with PE can be stratified in 3 groups according to the risk of recurrence : very low risk, high risk or Intermediate risk. Little is known about this last group.

Anticoagulation is efficient to prevent recurrence but is currently not recommended for patient with an intermediate risk of recurrence.

Identifying risk factors of recurrent PE remains a major issue to identify sub-groups of patients who would require lifelong anticoagulation.

In 30-40% of cases, PE patients develop residual pulmonary vascular obstruction (RPVO), which has been found to be associated with an increased recurrence risk. This last observation was mostly reported in patients with unprovoked PE (patients with high risk of recurrence) and RPVO was measured using conventional planar lung scan.

In patients with an intermediate risk of recurrence, the impact of RPVO has been much less studied. In addition, the definition of RPVO was variable according to studies and correlation between RPVO burden and recurrence risk has not been clearly demonstrated. This might be explained by the inherent limitation of RPVO quantification using conventional planar imaging, which is only based on a visual estimation on 2-dimensional images.

Ventilation/Perfusion Single Photon Emission Computed Tomography (V/Q SPECT/CT) is a new method of scintigraphic image acquisition that offers the advantage of 3-dimensional imaging, enabling more accurate and reproducible quantification of RPVO.

The main hypothesis of this study is that in patients with PE at intermediate risk of recurrence, RPVO computed with V/Q SPECT/CT imaging may be an important predictor of recurrence.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients ≥ 18 years, * who experienced an objectively proven PE, * who have been treated initially with anticoagulant therapy for 3 to 6 uninterrupted months (180 - 210 days) and for whom anticoagulation will not be prolonged. Exclusion Criteria: * Unwilling or unable to give written informed consent (protected adults, under tutorship or curatorship) * Patients deprived of their liberty by a judicial or administrative decision, patients undergoing psychiatric care by virtue of Articles L. 3212-1 and L. 3213-1 who are not covered by the provisions of Article L. 1121-8 and patients admitted to a health or social establishment for purposes other than research * No Social security affiliation * Isolated DVT * Pregnant women and parturients * Other indication for anticoagulant therapy (e.g. atrial fibrillation, mechanic valve) * Life expectancy \< 6 months * Any patients for whom there is a strong indication to treat longer than 6 months: * PE provoked by a major persistent factor (e.g. cancer) * Recurrent unprovoked PE PE provoked by a major transient risk factor (e.g. surgery with general anesthesia for greater than 30 min, confined to bed in hospital for at least 3 days with an acute illness, cesarean section) AND none of the following persistent factors : * BMI ≥ 30 * Chronic respiratory disease * Chronic inflammatory disease (e.g., ulcerative colitis, rheumatoid arthritis, etc.) * Hepatocellular insufficiency * Renal insufficiency with creatinine clearance \< 60 mL/min * Chronic or persistent immobilization

Primary outcome measure(s)

  • Symptomatic recurrent venous thromboembolism (VTE), including objectively confirmed nonfatal symptomatic PE or proximal deep vein thrombosis or fatal PE during a 24-month follow-up after inclusion in the study — From baseline to Month 24
    In case of a suspected VTE or death during follow-up, the study personnel will collect related clinical data on the electronic case report form, and prepare an adjudication file, including symptoms, clinical notes, hospital discharge summary, and results of all diagnostic tests. All suspicion of VTE recurrence will be adjudicated blindly by an independent central Clinical Events Committee. To assess the primary objective, RPVO will be defined by a perfusion mismatched defect of at least 5% of the whole lung, corresponding to a segmental defect. SPECT imaging should not be used at inclusion and should not result in proposing prolonged anticoagulation. SPECT images will be numerically stored and interpretation will be later performed independently by two nuclear medicine physicians who will be blinded to clinical history and the patient's outcome. Any difference in interpretation will be resolved by consensus.

Trial sites (13)

FacilityCityRegionStatus
CHU Amiens Amiens France Recruiting
CHU Angers Angers France Active Not Recruiting
CHU Brest Brest France Recruiting
Hôpital Louis MourierAP-HP Colombes France Recruiting
CHD Vendée - La Roche sur Yon La Roche-sur-Yon France Recruiting
Kremlin-Bicêtre AP-HP Le Kremlin-Bicêtre France Active Not Recruiting
CH Les Sables d'Olonne Les Sables-d'Olonne France Recruiting
Hegp Ap-Hp Paris France Recruiting
CH Quimper Quimper France Recruiting
CHU St-Etienne Saint-Etienne France Recruiting
CHIC Toulon Toulon France Recruiting
HIA Toulon Toulon France Recruiting
CHU Toulouse Toulouse France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06372730 on ClinicalTrials.gov ↗ ← All trials in France