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PROfunda Femoris Vein Thrombosis Evaluation and Clearance to Improve Outcomes of Endovascular Treatment for Acute Iliofemoral Deep Vein Thrombosis

31 sierpnia 2026 zaktualizowane przez: RenJi Hospital

PROfunda Femoris Vein Thrombosis Evaluation and Clearance to Improve Outcomes of Endovascular Treatment for Acute Iliofemoral Deep Vein Thrombosis: a Multicenter Randomized Controlled Study (The PROTECT Study)

Patients with iliofemoral vein thrombosis are prone to developing post-thrombotic syndrome (PTS). The profunda femoris vein (PFV) is an important inflow of the iliofemoral vein. Profunda femoris vein thrombosis clearance (PFV-TC) may improve the patency of iliofemoral vein and reduce the occurrence of PTS.

Przegląd badań

Szczegółowy opis

Acute lower extremity deep vein thrombosis (DVT) can lead to obstruction of veins, causing sudden lower limb swelling. Patients may also develop post-thrombotic syndrome (PTS) manifesting as recurrent lower limb swelling, skin disorders, and even non-healing ulcers, which severely affects the patient's quality of life. Among lower extremity DVT, thrombosis involving the iliofemoral veins is the most severe, with an incidence of PTS as high as 20%-50%. Percutaneous mechanical thrombectomy (PMT) utilizes mechanical aspiration to rapidly remove thrombus, relieve venous obstruction, and restore luminal patency. According to the results of a prospective clinical study, PMT can effectively improve the primary thrombus clearance rate and shorten hospital stay in patients with DVT. Among 329 patients, 192 (58.5%) achieved complete thrombus removal using the AngioJet catheter. PMT was once considered to be the first-line treatment option for DVT. However, the results of the ATTRACT study, published in 2017 in New England Journal of Medicine, sparked considerable controversy regarding the use of PMT for DVT. The ATTRACT study found that there was no significant difference in the incidence of PTS at two years after PMT compared with anticoagulation alone. Although PMT can rapidly remove thrombus, is it unable to improve the long-term outcomes for patients with DVT? According to previous studies, the primary patency rate at 12 months after PMT for acute iliofemoral venous thrombosis ranges from 77% to 85%, while the incidence of PTS at 24 months postoperatively is as high as 40%. Residual thrombus is an important cause of thrombus recurrence, re-occlusion of the vein, and poor clinical outcomes. Previous studies have primarily focused on thrombus clearance in the popliteal vein, superficial femoral vein, common femoral vein, and iliac vein, while neglecting the assessment and clearance of profunda femoris vein (PFV) thrombosis. As the PFV is an important inflow of the iliofemoral vein, whether PFV-TC can improve the patency rate and clinical outcomes of endovascular treatment for acute iliofemoral DVT remains unclear. In a preliminary study, the investigators analyzed and compared two cohorts: one receiving conventional endovascular treatment for acute iliofemoral venous thrombosis, and the other receiving conventional treatment combined with Profunda femoris vein thrombosis clearance (PFV-TC). The results showed that the 24-month patency rate of the iliofemoral vein was 90% vs. 72%, and the incidence of PTS was 11% vs. 32% (P<0.05). These findings were published in November 2025 in European Journal of Vascular and Endovascular Surgery. This study has garnered widespread attention, and de Wolf MAF published an invited commentary on this study, acknowledging the value of this approach in the endovascular treatment of acute iliofemoral DVT. Therefore, the investigators hypothesize that PFV-TC can improve inflow and reduce the incidence of PTS for iliofemoral DVT. However, high-level evidence is still lacking. The present study is a prospective, multicenter, randomized, open-label, evaluator-blinded, 1:1 parallel-controlled clinical trial investigating PFV-TC, aiming to obtain higher-level evidence to guide endovascular treatment of acute iliofemoral DVT.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

140

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

      • Shanghai, Chiny
        • Rekrutacyjny
        • Renji Hospital
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  1. Age ≥ 18 years and ≤ 85 years;
  2. Diagnosed with acute iliofemoral DVT involving iliac vein, common femoral vein, and the proximal segment (orifice) of PFV (confirmed by preoperative ultrasound, CT venography, or pre-procedural venography);
  3. Time from symptom onset to endovascular treatment ≤ 14 days;
  4. Patient receives endovascular treatment with PMT;
  5. Patient provides written informed consent.

Exclusion Criteria:

  1. Presence of pre-existing PTS in the limb scheduled for treatment, or a history of symptomatic DVT in the same limb;
  2. Concurrent symptomatic acute DVT involving the iliac vein and/or common femoral vein in the contralateral limb;
  3. Known allergy to heparin, low-molecular-weight heparin, contrast media, or other relevant agents;
  4. Concomitant severe pulmonary embolism with hemodynamic compromise, such as hypoxia or hypotension;
  5. Intolerance to endovascular intervention due to concurrent acute systemic illness, severe dyspnea, or other contraindications;
  6. Concomitant severe renal insufficiency with creatinine clearance < 30 ml/min;
  7. Presence of active bleeding, severe hepatic insufficiency, bleeding diathesis, or other coagulation disorders;
  8. Concomitant severe anemia (hemoglobin < 8.0 mg/dL) or thrombocytopenia (platelet count < 80,000/mL);
  9. History of subarachnoid hemorrhage, intracranial hemorrhage, intracranial vascular malformation, or intracranial aneurysm;
  10. Pregnancy;
  11. Presence of other diseases (e.g., advanced malignancy, cardiac insufficiency) with an estimated life expectancy < 24 months;
  12. Participation in another clinical trial of a drug or medical device within the past 1 month that may interfere with the present study;
  13. Unwillingness to participate in this trial.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: PMT with PFV-TC group
PMT with PFV-TC group (experimental group)
PMT with PFV-TC group (experimental group): Based on the control group, access is obtained via the contralateral common femoral vein using a crossover technique, or via a popliteal-profunda communicating vessel approach to PFV. The thrombus status of the PFV is assessed, and PMT is performed on the PFV thrombosis. After thrombectomy, venography is performed to evaluate the patency of the PFV. Successful PFV-TC is defined as the presence of continuous flow from the distal PFV to the CFV, including complete clearance (no residual thrombus) and partial clearance (continuous flow with residual thrombus). Conversely, the absence of continuous flow is defined as failed PFV-TC.
Aktywny komparator: PMT without PFV-TC group
PMT without PFV-TC group (control group)
An appropriate puncture approach is selected, including the ipsilateral calf vein, ipsilateral popliteal vein, or ipsilateral femoral vein. Under ultrasound guidance, a vascular sheath is inserted after puncture, and systemic heparinization is performed. Using a guidewire and catheter, the guidewire is advanced antegradely into the inferior vena cava to establish a pathway. After the pathway is established, PMT is performed using a mechanical thrombectomy device. Acceptable thrombectomy devices include commercially available mechanical aspiration thrombectomy devices such as the AngioJet catheter (Boston Scientific, USA) and the Indigo catheter (Penumbra Inc, USA). After thrombectomy, the outcome is evaluated by venography. If iliac vein stenosis greater than 50% is detected, balloon dilation is performed using a balloon matched to the normal vessel diameter. If residual stenosis remains greater than 50% after balloon dilation, stent implantation is performed.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Incidence of Post-Thrombotic Syndrome (PTS)
Ramy czasowe: at 24 months
Assessed by the Villalta score. The Villalta scale is the recommended tool for diagnosing and grading the severity of PTS. It is a composite score based on 11 items (5 patient-reported symptoms and 6 clinician-assessed signs), each rated from 0 (absent) to 3 (severe), yielding a total score ranging from 0 to 33. A score of 0-4 indicates no PTS, whereas a score of ≥5 or venous ulcer confirms the diagnosis of PTS. Specifically, scores of 5-9 indicate mild PTS, 10-14 indicate moderate PTS, and a score of ≥15 or venous ulcer indicates severe PTS. Higher scores reflect greater disease severity.
at 24 months

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Incidence of moderate-to-severe PTS
Ramy czasowe: at 6, 12, and 24 months
Assessed by the Villalta score
at 6, 12, and 24 months
Patency rate of the ipsilateral iliofemoral vein
Ramy czasowe: at 12 months and 24 months
Assessed by color Doppler ultrasound
at 12 months and 24 months
Recurrence rate of symptomatic Deep Vein Thrombosis (DVT)
Ramy czasowe: at 24 months
Assessed by symptoms combined with ultrasound examination in the ipsilateral limb
at 24 months
Rate of re-intervention
Ramy czasowe: at 24 months
Assessed by documentation of clinical reintervention
at 24 months
Incidence of PTS
Ramy czasowe: at 6 and 12 months
Assessed by the Villalta score
at 6 and 12 months
Quality of life score
Ramy czasowe: at 6, 12, and 24 months
Assessed by Venous Insufficiency Epidemiological and Economic Study Quality of Life questionnaire (VEINES-QOL). The minimum value is 0 and the maximum value is 100. Higher score means a better outcome.
at 6, 12, and 24 months

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Incidence of major bleeding
Ramy czasowe: at 24 months
Defined by International Society on Thrombosis and Haemostasis (ISTH) criteria
at 24 months
Incidence of symptomatic Pulmonary Embolism (PE)
Ramy czasowe: at 24 months
Assessed by symptoms combined with contrast-enhanced computed tomography examination
at 24 months
Incidence of symptomatic Venous Thromboembolism (VTE)
Ramy czasowe: at 24 months
Assessed by symptoms combined with ultrasound and contrast-enhanced computed tomography examination
at 24 months
All-cause mortality
Ramy czasowe: at 24 months
All-cause death
at 24 months

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

24 czerwca 2026

Zakończenie podstawowe (Szacowany)

30 czerwca 2029

Ukończenie studiów (Szacowany)

31 grudnia 2029

Daty rejestracji na studia

Pierwszy przesłany

26 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

26 maja 2026

Pierwszy wysłany (Rzeczywisty)

3 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

2 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

31 sierpnia 2026

Ostatnia weryfikacja

1 sierpnia 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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