- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07857850
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.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Shanghai, Kina
- Shanghai Pudong Hospital
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Fujian
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Xiamen, Fujian, Kina
- Xiamen Cardiovascular Hospital Xiamen University
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Guangzhou
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Guangzhou, Guangzhou, Kina
- The First Affiliated Hospital of Guangzhou Medical University
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Jiangsu
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Suzhou, Jiangsu, Kina
- The Second Affiliated Hospital of Soochow University
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Shaanxi
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Xi'an, Shaanxi, Kina
- The First Affiliated Hospital of Xi'an Jiaotong University
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Shandong
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Qingdao, Shandong, Kina
- The Affiliated Hospital of Qingdao University
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Subjects aged between 18 and 80 years.
- Patients diagnosed with deep venous thrombosis (DVT) within 30 days of onset via color Doppler ultrasound (CDUS) or CT venography (CTV) imaging.
- Target lesions involving the inferior vena cava, common iliac vein, external iliac vein, common femoral vein, superficial femoral vein, or popliteal vein.
- 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:
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Patients diagnosed with chronic-phase deep venous thrombosis (DVT) (symptom onset >30 days).
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Patients with bilateral lower extremity DVT requiring thrombus removal in both limbs.
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Patients with known bleeding disorders or bleeding tendencies (platelet count <50×10⁹/L or INR >3).
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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).
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History of heart failure, stroke, and/or myocardial infarction within 1 month, or planned coronary/carotid revascularization or major cardiovascular/cerebrovascular surgery.
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Target lesions involving veins with a diameter <3 mm.
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Patients with a life expectancy <12 months (e.g., malignancy).
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Patients with congenital inferior vena cava (IVC) hypoplasia/malformation or other congenital IVC/iliac vein abnormalities.
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Allergy to anticoagulants or iodine-based contrast agents.
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Bedridden patients unlikely to regain limb mobility within 1 month post-procedure.
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Patients with pre-existing venous stents or IVC filters that may interfere with device deployment.
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Patients with recurrent ipsilateral DVT.
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Pregnant or lactating women.
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High-risk pulmonary thromboembolism (PTE) (manifested by shock/hypotension: systolic blood pressure <90 mmHg or >40 mmHg drop from baseline lasting >15 minutes).
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Severe post-thrombotic syndrome (PTS) (defined as Villalta score >14 points and/or skin ulcers).
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Patients who underwent percutaneous mechanical thrombectomy within 1 month.
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Contraindications to anticoagulation (e.g., heparin-induced thrombocytopenia [HIT]).
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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.
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History of nickel-titanium (Nitinol) alloy allergy.
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Participation in other ongoing drug/device clinical trials.
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Patients deemed ineligible by the investigator.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Thrombus clearance rate
Tidsramme: immediately after the surgery
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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
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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thrombus recurrence rate
Tidsramme: 1, 3, and 6 months
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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
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Post-thrombotic syndrome (PTS)
Tidsramme: 1, 3, and 6 months
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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
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Device success
Tidsramme: immediately after the surgery
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Successful delivery of the thrombectomy device to the target lesion, successful deployment, and successful withdrawal of the delivery system. |
immediately after the surgery
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Procedural success
Tidsramme: immediately after the surgery
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Immediate post-procedure thrombus clearance rate of Grade II or above and no major adverse event before discharge |
immediately after the surgery
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Venous Clinical Severity Score (VCSS)
Tidsramme: 1, 3, and 6 months
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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
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Chronic Venous Insufficiency Questionnaire (CIVIQ-20) score
Tidsramme: 1, 3, and 6 months
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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
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Major adverse events (MAE) at 30 days
Tidsramme: 30 days
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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
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Adverse event rate within 12 months after surgery
Tidsramme: 12 months after surgery
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Adverse event rate within 12 months after surgery |
12 months after surgery
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Serious adverse event rate within 12 months after surgery
Tidsramme: 12 months after surgery
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Serious adverse event rate within 12 months after surgery |
12 months after surgery
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Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- TF02-001A
Plan for individuelle deltagerdata (IPD)
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