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A Prospective, Multicenter, Single-Arm Trial of Peripheral Vein Thrombectomy Stent System in Deep Venous Thrombosis

A Prospective, Multicenter, Single-Arm Trial to Evaluate the Safety and Efficacy of the Peripheral Vein Thrombectomy Stent System in the Treatment of Deep Venous Thrombosis

To evaluate the safety and efficacy of peripheral vein thrombectomy stent system produced by Shanghai Tendfu Medical Technology Co., Ltd. in the treatment of acute or subacute deep venous thrombosis.

調査の概要

詳細な説明

This project is being conducted at qualified clinical research institutions, where investigators are using a thrombectomy device developed by Shanghai Tengfu Medical Technology Co., Ltd. to treat subjects with deep vein thrombosis; it is a prospective, multicenter, single-arm clinical study utilizing a target performance value design, with subject enrollment managed via an online registration system. The primary endpoint-thrombectomy efficacy rate assessed immediately post-procedure-is used to determine whether the investigational device meets the efficacy standard, while device efficacy is further evaluated by the recurrence rate of thrombosis at the target lesion at 1, 3, and 6 months post-procedure, the incidence of post-thrombotic syndrome at 1, 3, and 6 months, device success rate, procedural success rate, and Venous Clinical Severity Score (VCSS) and Chronic Venous Insufficiency Questionnaire (CIVIQ-20) scores at 1, 3, and 6 months. Device safety is assessed based on the incidence of Major Adverse Events (MAEs) at 30 days post-procedure, as well as the incidence of adverse events and serious adverse events at 1, 3, and 6 months post-procedure.

研究の種類

介入

入学 (実際)

132

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Shanghai、中国
        • Shanghai Pudong Hospital
    • Fujian
      • Xiamen、Fujian、中国
        • Xiamen Cardiovascular Hospital Xiamen University
    • Guangzhou
      • Guangzhou、Guangzhou、中国
        • The First Affiliated Hospital of Guangzhou Medical University
    • Jiangsu
      • Suzhou、Jiangsu、中国
        • The Second Affiliated Hospital of Soochow University
    • Shaanxi
      • Xi'an、Shaanxi、中国
        • The First Affiliated Hospital of Xi'an Jiaotong University
    • Shandong
      • Qingdao、Shandong、中国
        • The Affiliated Hospital of Qingdao University

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~80年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  1. Subjects aged between 18 and 80 years.
  2. Patients diagnosed with deep venous thrombosis (DVT) within 30 days of onset via color Doppler ultrasound (CDUS) or CT venography (CTV) imaging.
  3. Target lesions involving the inferior vena cava, common iliac vein, external iliac vein, common femoral vein, superficial femoral vein, or popliteal vein.
  4. Subjects capable of understanding the purpose of the trial, who voluntarily participate and sign an informed consent form, and are willing to undergo follow-up evaluations.

Exclusion Criteria:

  1. Patients diagnosed with chronic-phase deep venous thrombosis (DVT) (symptom onset >30 days).

  2. Patients with bilateral lower extremity DVT requiring thrombus removal in both limbs.

  3. Patients with known bleeding disorders or bleeding tendencies (platelet count <50×10⁹/L or INR >3).

  4. Severe hepatic or renal dysfunction Renal insufficiency (estimated glomerular filtration rate [GFR] <30 mL/min); Active liver disease or ALT >3 × upper limit of normal (ULN).

  5. History of heart failure, stroke, and/or myocardial infarction within 1 month, or planned coronary/carotid revascularization or major cardiovascular/cerebrovascular surgery.

  6. Target lesions involving veins with a diameter <3 mm.

  7. Patients with a life expectancy <12 months (e.g., malignancy).

  8. Patients with congenital inferior vena cava (IVC) hypoplasia/malformation or other congenital IVC/iliac vein abnormalities.

  9. Allergy to anticoagulants or iodine-based contrast agents.

  10. Bedridden patients unlikely to regain limb mobility within 1 month post-procedure.

  11. Patients with pre-existing venous stents or IVC filters that may interfere with device deployment.

  12. Patients with recurrent ipsilateral DVT.

  13. Pregnant or lactating women.

  14. High-risk pulmonary thromboembolism (PTE) (manifested by shock/hypotension: systolic blood pressure <90 mmHg or >40 mmHg drop from baseline lasting >15 minutes).

  15. Severe post-thrombotic syndrome (PTS) (defined as Villalta score >14 points and/or skin ulcers).

  16. Patients who underwent percutaneous mechanical thrombectomy within 1 month.

  17. Contraindications to anticoagulation (e.g., heparin-induced thrombocytopenia [HIT]).

  18. Contraindications to thrombolysis:

    Allergy to thrombolytic agents; High bleeding risk or active bleeding within 2 - 4 weeks (e.g., intracranial, gastrointestinal, or urinary tract hemorrhage); Recent major surgery, biopsy, CPR, or non-compressible puncture; Severe trauma within 2 - 4 weeks; Uncontrolled hypertension (>160/110 mmHg); Bacterial endocarditis; Aortic dissection, aneurysm, or arteriovenous malformation.

  19. History of nickel-titanium (Nitinol) alloy allergy.

  20. Participation in other ongoing drug/device clinical trials.

  21. Patients deemed ineligible by the investigator.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Peripheral Vein Thrombectomy Stent System

Tendfast™ Peripheral Vein Thrombectomy Stent System

Tendfast™ Peripheral Vein Thrombectomy Stent System (Tendfast™) is a mechanical thrombectomy system consisting of a peripheral vein thrombectomy stent and a thrombus aspiration catheter. Guided by a guidewire, the stent is delivered to the thrombus, deployed against the vessel wall to engage, scrape, and collect the thrombus into its mesh for removal, after which manual negative-pressure aspiration through the catheter clears residual thrombus and restores blood flow.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Thrombus clearance rate
時間枠:immediately after the surgery

Thrombus clearance (immediately post-procedure): The thrombus clearance rate is divided into 3 grades: Grade I is <50%; Grade II is 50%-95%; Grade III is >95%. The lower extremity veins are divided into 7 segments: inferior vena cava, common iliac vein, external iliac vein, common femoral vein, proximal superficial femoral vein, distal superficial femoral vein, and popliteal vein. Pre- and post-procedure luminal patency is visually assessed by venography: a patent lumen is scored as 0 points, partial occlusion (<50%) as 1 point, severe occlusion (50%-95%) as 2 points, and complete occlusion (95%-100%) as 3 points. The formula for the thrombus clearance rate is: (preoperative venous patency score - postoperative venous patency score) / preoperative venous patency score × 100%. A thrombus clearance rate of Grade II or above is considered effective.

immediately after the surgery

二次結果の測定

結果測定
メジャーの説明
時間枠
thrombus recurrence rate
時間枠:1, 3, and 6 months

Compared with before discharge, worsening of symptoms with imaging confirmation that the target lesion thrombus occludes the vessel or interrupts blood flow, requiring repeat intervention.

1, 3, and 6 months
Post-thrombotic syndrome (PTS)
時間枠:1, 3, and 6 months

Occurrence and severity grading assessed by the Villalta score. PTS is defined as a Villalta score >4. The Villalta score includes 5 symptoms (pain, muscle cramps, heaviness, paresthesia, itching) and 6 signs (pretibial edema, pigmentation, lipodermatosclerosis, redness of the skin, superficial venous dilatation, calf muscle tenderness). Severity is classified as mild (5-9), moderate (10-14), and severe (>14 and/or presence of skin ulcer).

1, 3, and 6 months
Device success
時間枠:immediately after the surgery

Successful delivery of the thrombectomy device to the target lesion, successful deployment, and successful withdrawal of the delivery system.

immediately after the surgery
Procedural success
時間枠:immediately after the surgery

Immediate post-procedure thrombus clearance rate of Grade II or above and no major adverse event before discharge

immediately after the surgery
Venous Clinical Severity Score (VCSS)
時間枠:1, 3, and 6 months

Evaluation of clinical symptoms by comparing improvement from baseline to post-treatment. VCSS includes 10 clinical elements (pain, varicose veins, edema, skin pigmentation, inflammation, induration, number of active ulcers, ulcer size, and use of compression therapy), each scored 0-3 by severity, with a total score of 30.

1, 3, and 6 months
Chronic Venous Insufficiency Questionnaire (CIVIQ-20) score
時間枠:1, 3, and 6 months

Improvement/change compared with pre-operation based on the CIVIQ-20 score. CIVIQ is a specific, self-administered quality-of-life questionnaire for patients with chronic venous disease of the lower extremities. It includes 20 items across 4 domains-social, psychological, physical, and pain-and mainly reflects the impact of chronic venous insufficiency on patients' quality of life.

1, 3, and 6 months
Major adverse events (MAE) at 30 days
時間枠:30 days

all-cause death, major bleeding, new-onset symptomatic pulmonary embolism, and target lesion thrombus recurrence. Major bleeding is defined as intracranial hemorrhage or severe bleeding that leads to death, surgery, discontinuation of treatment, or transfusion. Transfusion [15] is defined as two or more units of whole blood (400 mL) or red blood cells (240 mL). Symptomatic pulmonary embolism is defined as pulmonary embolism with clinical symptoms such as dyspnea, chest pain, hemoptysis, panic, cough, or syncope. Target lesion thrombus recurrence is defined as worsening symptoms compared with before discharge, with imaging confirmation that the target lesion thrombus occludes the vessel or interrupts blood flow and requires repeat intervention.

30 days
Adverse event rate within 12 months after surgery
時間枠:12 months after surgery

Adverse event rate within 12 months after surgery

12 months after surgery
Serious adverse event rate within 12 months after surgery
時間枠:12 months after surgery

Serious adverse event rate within 12 months after surgery

12 months after surgery

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2022年8月1日

一次修了 (実際)

2023年8月30日

研究の完了 (実際)

2023年8月30日

試験登録日

最初に提出

2026年9月29日

QC基準を満たした最初の提出物

2026年10月2日

最初の投稿 (実際)

2026年10月5日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月5日

QC基準を満たした最後の更新が送信されました

2026年10月2日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • TF02-001A

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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