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- Ensaio Clínico NCT07622199
PROfunda Femoris Vein Thrombosis Evaluation and Clearance to Improve Outcomes of Endovascular Treatment for Acute Iliofemoral Deep Vein Thrombosis
31 de agosto de 2026 atualizado por: 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.
Visão geral do estudo
Status
Recrutamento
Condições
Descrição detalhada
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.
Tipo de estudo
Intervencional
Inscrição (Estimado)
140
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Qihong Ni
- Número de telefone: +8615801900772
- E-mail: niqihong1989@163.com
Locais de estudo
-
-
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Shanghai, China
- Recrutamento
- Renji Hospital
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Contato:
- Qihong Ni
- Número de telefone: +8615801900772
- E-mail: niqihong1989@163.com
-
-
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Não
Descrição
Inclusion Criteria:
- Age ≥ 18 years and ≤ 85 years;
- 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);
- Time from symptom onset to endovascular treatment ≤ 14 days;
- Patient receives endovascular treatment with PMT;
- Patient provides written informed consent.
Exclusion Criteria:
- Presence of pre-existing PTS in the limb scheduled for treatment, or a history of symptomatic DVT in the same limb;
- Concurrent symptomatic acute DVT involving the iliac vein and/or common femoral vein in the contralateral limb;
- Known allergy to heparin, low-molecular-weight heparin, contrast media, or other relevant agents;
- Concomitant severe pulmonary embolism with hemodynamic compromise, such as hypoxia or hypotension;
- Intolerance to endovascular intervention due to concurrent acute systemic illness, severe dyspnea, or other contraindications;
- Concomitant severe renal insufficiency with creatinine clearance < 30 ml/min;
- Presence of active bleeding, severe hepatic insufficiency, bleeding diathesis, or other coagulation disorders;
- Concomitant severe anemia (hemoglobin < 8.0 mg/dL) or thrombocytopenia (platelet count < 80,000/mL);
- History of subarachnoid hemorrhage, intracranial hemorrhage, intracranial vascular malformation, or intracranial aneurysm;
- Pregnancy;
- Presence of other diseases (e.g., advanced malignancy, cardiac insufficiency) with an estimated life expectancy < 24 months;
- Participation in another clinical trial of a drug or medical device within the past 1 month that may interfere with the present study;
- Unwillingness to participate in this trial.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of Post-Thrombotic Syndrome (PTS)
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of moderate-to-severe PTS
Prazo: at 6, 12, and 24 months
|
Assessed by the Villalta score
|
at 6, 12, and 24 months
|
|
Patency rate of the ipsilateral iliofemoral vein
Prazo: at 12 months and 24 months
|
Assessed by color Doppler ultrasound
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at 12 months and 24 months
|
|
Recurrence rate of symptomatic Deep Vein Thrombosis (DVT)
Prazo: at 24 months
|
Assessed by symptoms combined with ultrasound examination in the ipsilateral limb
|
at 24 months
|
|
Rate of re-intervention
Prazo: at 24 months
|
Assessed by documentation of clinical reintervention
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at 24 months
|
|
Incidence of PTS
Prazo: at 6 and 12 months
|
Assessed by the Villalta score
|
at 6 and 12 months
|
|
Quality of life score
Prazo: at 6, 12, and 24 months
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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.
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at 6, 12, and 24 months
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of major bleeding
Prazo: at 24 months
|
Defined by International Society on Thrombosis and Haemostasis (ISTH) criteria
|
at 24 months
|
|
Incidence of symptomatic Pulmonary Embolism (PE)
Prazo: at 24 months
|
Assessed by symptoms combined with contrast-enhanced computed tomography examination
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at 24 months
|
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Incidence of symptomatic Venous Thromboembolism (VTE)
Prazo: at 24 months
|
Assessed by symptoms combined with ultrasound and contrast-enhanced computed tomography examination
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at 24 months
|
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All-cause mortality
Prazo: at 24 months
|
All-cause death
|
at 24 months
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
24 de junho de 2026
Conclusão Primária (Estimado)
30 de junho de 2029
Conclusão do estudo (Estimado)
31 de dezembro de 2029
Datas de inscrição no estudo
Enviado pela primeira vez
26 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
26 de maio de 2026
Primeira postagem (Real)
3 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
2 de setembro de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
31 de agosto de 2026
Última verificação
1 de agosto de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- The PROTECT Study
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .