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临床试验/NCT04128956
NCT04128956终止2 期

Aspirin® Plus Rivaroxaban Versus Rivaroxaban Alone for the Prevention of Venous Stent Thrombosis in Patients With Post-thrombotic Syndrome a Multi-center, International, Randomized, Open Label, Controlled Trial

University of Zurich6 个研究点 分布在 3 个国家目标入组 172 人开始时间: 2020年3月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
172
试验地点
6
主要终点
The primary patency rate is defined as the percentage of patients with primary treatment success after 6 months

研究概览

简要总结

To show if a combination therapy of rivaroxaban plus Aspirin® is more efficient (superiority testing) as rivaroxaban alone in the prevention of early venous stent thrombosis in patients suffering from post-thrombotic syndrome in the first 6 months following endovascular therapy To demonstrate tolerability of combination therapy of Aspirin® plus rivaroxaban in long-term treatment.

详细描述

Deep vein thrombosis is associated with severe morbidity and mortality. It is the most frequent type of venous thromboembolism (VTE) and responsible for approximately 800.000 deaths per year in the European Union and the United States combined. The post-thrombotic syndrome (PTS) is a frequent long-term complication of proximal deep vein thrombosis (DVT), which occurs in up to 50% of patients despite adequate anticoagulation therapy and compression stockings. Patients with DVT of the inferior vena cava or iliac veins are at highest risk for the development of PTS. Inadequate recanalization and persistent venous outflow obstruction promotes the development of venous hypertension, secondary valve damage, valvular reflux, and the clinical manifestation of PTS, which consists of a similar set of signs and symptoms as in superficial venous insufficiency. Symptoms may include leg edema, pruritus, dysesthesia, leg pain on standing, skin changes, venous claudication with limited exercise capacity, and leg ulcers. Venous ulcers occur in approximately 10% of patients with iliofemoral DVT after 3 years.

The diagnosis of PTS is made based on the presence of its clinical features, a prior history of proximal DVT, and the results of imaging studies. Clinical scores, such as the Villalta score, can function as a tool to stage severity of disease. PTS in classified as mild if the Villalta score is 5-9, moderate if the Villalta score is 10-14, and severe if the Villata score exceeds 15 points. Disabling venous claudication can be diagnosed by treadmill exercise tests. Magnetic resonance imaging venography can be used in addition to duplex ultrasound to objectify central venous obstruction, and unmark underlying strategic compression sides (e.g. May-Thurner syndrome).

Recommendations by the American Heart Association for endovascular treatment of PTS suggest percutaneous recanalization including the implantation of stents for symptomatic patients) Endovascular therapy with provisional stent placement shows promising clinical outcomes to improve PTS-associated symptoms, including leg ulcers. However, there is significant risk for early stent thrombosis, estimated as high as 21% after 12 months.

Antithrombotic therapy is the corner stone of the prevention of stent thrombosis, but there is great inconsistency in the use of antithrombotic agents. The value of extended anticoagulation therapy in PTS patients beyond the durations recommended in VTE management guidelines is controversial, and it has not been specifically investigated in the presence of venous stent implants. Although oral anticoagulants are accepted as the main therapy regimen, the benefit of antiplatelet therapy (APT) in the early phase after venous stent implantation is unclear.

According to a recent international survey completed by 106 experts, one third reported to use life-long anticoagulation with a vitamin-K antagonist (VKA), and another 19% chose life-long anticoagulation with direct anticoagulant (DOAC) for a presented case scenario of a PTS patients treated with venous stents. The use of APT following stent placement alone or in combination with an anticoagulant was reported in 7% and 13%, respectively, whereas 25% reported use of APT following discontinuation of ACT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed informed consent form and data protection declaration obtained prior to any trial-specific procedures
  • Patient aged ≥18 years
  • Confirmed diagnosis of post-thrombotic syndrome defined as Villalta score > 4 points prior to enrolment and venous stent intervention
  • Confirmed stenosis of inferior vena cava, iliac vein, or common femoral vein by duplex ultrasound or cross-sectional imaging (CT venography or MR venography) prior to enrolment and venous stent intervention
  • Successfully conducted venous stent intervention involving either:
  • inferior vena cava
  • iliac vein or
  • common femoral vein
  • Patients either on active treatment with rivaroxaban or patients planned for treatment with rivaroxaban after intervention

排除标准

  • Previous venous intervention in target vessels
  • Any contraindication for antithrombotic therapy (e.g. active gastric ulcer, duodenal ulcer, bleeding disorder with increased tendency of bleedings)
  • Patients with a recent (3 months) clinically significant bleeding and / or active or recent (3 months) ulcerative or inflammatory gastrointestinal disease
  • Ongoing antiplatelet therapy or previous antiplatelet therapy within 7 days prior to Visit 1
  • Acute thrombosis (venous thromboembolism events < 3 months prior to Visit 1)
  • Pre-existing coagulopathy
  • Prior stroke or transient ischemic attack (< 12 months prior to Visit 1)
  • Pregnancy, breast feeding, or planned pregnancy within the trial period or women of childbearing potential not using an adequate method of contraception
  • Severe heart, liver or kidney disease
  • Severe somatopathic, neurological and / or psychiatric disease(s)
  • Malignant growth (concurrent or previous cancer with a relapse-free and treatment-free interval of less than 5 years before Visit 1)
  • Known hypersensitivity to acetylsalicylic acid (Aspirin® cardio or Aspirin® protect and / or its excipients), to other antiphlogistic drugs or to analgesics or anti-fever drugs
  • Concomitant intake of Methotrexat > 15 mg per week
  • Parallel participation in another clinical trial, participation in a clinical trial within less than 6 weeks prior to the Screening visit or previous participation in this clinical trial
  • Known to be, or suspected of being unable to comply with the trial protocol (e.g. no permanent address, history of drug abuse, known to be non-compliant or presenting an unstable psychiatric history)
  • Legal incapacity and / or other circumstances rendering the patient unable to understand the nature, scope and possible impact of the study
  • Custody by juridical or official order
  • Evidence of an uncooperative attitude
  • Difficulties in understanding the language in which the patient information is given
  • Patients dependent from the investigator or sponsor (e.g. close relatives of the investigator, employees of the clinic, the sponsor or involved CRO(s))

研究组 & 干预措施

Aspirin®

Experimental

To show if a combination therapy of rivaroxaban plus Aspirin® is more efficient (superiority testing) as rivaroxaban alone in the prevention of early venous stent thrombosis in patients suffering from post-thrombotic syndrome in the first 6 months following endovascular therapy.

To demonstrate tolerability of combination therapy of Aspirin® plus rivaroxaban in long-term treatment.

干预措施: Aspirin 100mg (Drug)

结局指标

主要结局

The primary patency rate is defined as the percentage of patients with primary treatment success after 6 months

时间窗: 6 month

The primary patency rate is defined as the percentage of patients with primary treatment success after 6 months (=Visit 3), i.e. without the occurrence of either i) occlusion of at least a part of the stent segment or ii.) a re-intervention to maintain patency of the treated segment.

次要结局

  • Revised venous clinical severity score (rVCSS)(3 and 6 months)
  • Difference of limb circumference(3 and 6 months)
  • Secondary patency rate after 3 and 6 months(3 and 6 months)
  • Change in Villalta score(3 and 6 months)
  • Primary patency rate after 3 months(3 month)
  • Primary sustained clinical success after 3 and 6 months (=Visit 2 and Visit 3)(3 and 6 months)
  • Difference between treatment groups in the incidence of patients with open stents but >50% residual stenosis according Duplex criteria(3 month)
  • Quality of life using the CIVIQ-20 (chronic venous insufficiency quality of life questionnaire)(3 and 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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