Skip to main content
OpenTrials
Completed

NCT Number: NCT05827120

Endovascular Therapy in Patients With Acute Deep Vein Thrombosis

Despite optimal anticoagulation therapy of patients with proximal deep vein thrombosis (DVT), there is still high number of patients suffering from post-thrombotic syndrome (PTS) due to the chronic venous occlusion, suboptimal collateralization, and venous valvular dysfunction. Last two decades endovascular catheter-based treatment modalities have been tested and used in an attempt to reduce incidence and symptoms of PTS in selected patients.

Especially, patients with extensive iliofemoral DVT have an increased risk of PTS. In an effort to accelerate thrombus dissolution or thrombus extraction, the endovascular removal of acute venous thrombus has been introduced as therapeutic option in patients with extensive iliofemoral DVT.

Randomized trials of catheter-based strategies for thrombus removal have documented improved vein patency, preserved valves function, and reduced post-thrombotic syndrome.

The aim of our study is to evaluate the safety and efficacy of different types of endovascular methods of treatment followed by anticoagulation therapy in patients with acute extensive DVT. Retrospective multicentre analysis of app 100 patients scheduled for endovascular treatment of extensive DVT. The results of mechanical/pharmacomechanical thrombectomy followed by local catheter directed thrombolysis (CDT), will be compared with CDT alone, or with ultrasound-accelerated thrombolysis. The 24-month incidence of PTS assessed by Villalta scoring system, major bleeding complications, the rate of venous recanalization, recurrence of DVT, and other end-points will be evaluated.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Central Slovakia Institute of Cardiovascular Diseases in Banská Bystrica, Banská Bystrica, Slovakia

Loading trial locations.

About this study

Aim: The aim of the study is to evaluate the long-term incidence of PTS in patients treated by different endovascular methods and protocols in combination with anticoagulation medication in patients with acute extensive DVT.

Hypothesis: Mechanical / pharmacomechanical thrombectomy (PMT) following by CDT and further anticoagulation therapy is safe and effective mode of acute DVT treatment with reduction of PTS after 24 months in comparison with historical data and with other modes of endovascular therapy.

Methods: Retrospective multicentre analysis of patients scheduled to interventional endovenous treatment of extensive DVT.

The major end-point:

  • The development of PTS during the 24-month follow-up period

The minor end-points:

  • The occurrence of major bleeding and live-threatening bleeding episodes
  • The development of PTS during the 6-month and 12-month follow-up period
  • The rate of venous recanalization after intervention assessed by ultrasound
  • The occurrence of pulmonary embolism
  • Recurrence of DVT
  • Mortality, myocardial infarction, stroke during follow-up

The occurrence of PTS will be assessed by clinical evaluation and by Villalta scoring system.

Patients suitable for endovascular therapy and for enrolment into study:

  • first episode of acute iliofemoral DVT
  • duration of symptoms <14 days
  • symptomatic patients with no or limited response to initial anticoagulation therapy in terms of symptomatology and signs of recanalization
  • low bleeding risk
  • good functional capacity and life expectancy

Endovascular procedures retrospectively analysed:

  • Catheter directed thrombolysis (CDT): dedicated infusion catheter with side holes is placed across the acute thrombus, and slow, continuous infusion (through the catheter, or both through the catheter and sheath) of a chemical thrombolysis agent is initiated (alteplase 1mg per hour simultaneously with unfractionated heparine (UFH) in anticoagulation dosage); activated partial thromboplastin time (APTT), fibrinogen (Fbg), and blood count must be controlled;
  • Mechanical thrombectomy: mechanical aspiration of fresh thrombus; mostly followed by CDT;
  • Pharmacomechanical thrombectomy (PMT): combination of some form of mechanical disruption of the thrombus in conjunction with chemical lysis. There is evidence that PMT quickens thrombolysis compared with CDT alone. Dedicated devices combining chemical thrombolysis via power-pulse fluid plus plasminogen activator thrombus penetration, with rheolytic fluid-based disruption of thrombus and catheter-based aspiration thrombectomy.
  • Ultrasound-accelerated thrombolysis combines chemical CDT with low-power high-frequency ultrasound application to the proprietary infusion catheter/wire combination, with the ultrasonic vibration purported to hasten thrombus disruption; the addition of ultrasound during lytic infusion increases the surface area of the fibrin, thereby permitting more efficient binding of the plasminogen activator to the fibrin-bound plasminogen
  • Stenting of residual thrombotic lesions, and stenting of common iliac vein compression in the presence of May-Thurner syndrome;

Peri-procedure and post-procedure care retrospectively analysed:

  • continuous in-hospital monitoring to minimize CDT-related complications;
  • APTT, Fbg concentration, and blood count are monitored;
  • Anticoagulation after endovascular procedure as standard regimen, if no contraindications, mostly during the 6-month time period; longer anticoagulation regimen is at discretion of treated centre and physician;
  • after venous stenting may be consider clopidogrel along with anticoagulation therapy for 1 month (not proven); Ultrasound evaluation during follow-up (data from documentation)
  • recanalization - no residual thrombosis
  • recanalization >50%
  • recanalization <50%
  • minimal US signs of recanalization/no recanalization Post-thrombotic syndrome: clinical evaluation and/or Villalta score
  • No PTS: Villalta <5 points
  • Mild: 5-9 points
  • Moderate: 10-14 points
  • Severe PTS: ≥15 points/venous ulcer

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • first episode of acute iliofemoral DVT
  • duration of symptoms <14 days
  • symptomatic patients with no or limited response to initial anticoagulation therapy in terms of symptomatology and signs of recanalization
  • low bleeding risk
  • good functional capacity and life expectancy

Exclusion criteria

  • - presence of malignity (2 centers out of 3)
  • pregnancy
  • haemorrhagic diathesis / high risk of bleeding
  • negative prognosis of survival
  • renal / hepatic failure
  • chronic course of DVT

Treatment and study plan

Mechanical / pharmacomechanical thrombectomy plus local catheter directed thrombolysis

Device
  • Catheter directed thrombolysis (CDT): dedicated thrombolytic catheter with side holes is placed across the acute thrombus, and slow, continuous infusion (through the catheter, or both through the catheter and sheath) of a chemical thrombolysis agent is applied - alteplase 1mg/hour plus unfractionated heparine in anticoagulation dosage;
  • Mechanical thrombectomy: mechanical aspiration of fresh thrombus;
  • Pharmacomechanical thrombectomy (PMT): combination of mechanical disruption of the thrombus, and its aspiration, with simultaneous application of alteplase via dedicated catheter - instilation of acute/subacute thrombus with its subsequent aspiration;

Local catheter directed thrombolysis alone

Device
  • Catheter directed thrombolysis (CDT): dedicated thrombolytic catheter with side holes is placed across the acute thrombus, and slow, continuous infusion (through the catheter, or both through the catheter and sheath) of a chemical thrombolysis agent is applied - alteplase 1mg/hour plus unfractionated heparine in anticoagulation dosage;

Primary outcomes

  1. Post-thrombotic syndrome

    Time frame: 24-month follow-up period

    The occurrence of PTS will be assessed by clinical evaluation and by Villalta scoring system (0-33), higher scores mean a worse outcome.

Secondary outcomes

  1. The occurrence of major bleeding and live-threatening bleeding episodes

    Time frame: periprocedural, in-hospital (up to day 7), 24 months

    clinical and laboratory evaluation of bleeding

  2. The development of PTS during the 6-month and 12-month follow-up period

    Time frame: 6-month and 12-month follow-up period

    The occurrence of PTS will be assessed by clinical evaluation and by Villalta scoring system (0-33), higher scores mean a worse outcome.

  3. The rate of venous recanalization after intervention

    Time frame: early - in-hospital (up to day 7), 6-month

    assessed by ultrasound

  4. The occurrence of pulmonary embolism

    Time frame: early - in-hospital (up to day 7), 12-month, 24-month follow-up

    clinical evaluation

  5. Recurrence of DVT

    Time frame: 12-month, 24-month follow-up

    clinical and ultrasound evaluation

  6. Mortality, MI, stroke during follow-up

    Time frame: In-hospital (up to day 7), 12-month, 24-month follow-up

    history assessment

Sponsors and collaborators

Lead sponsor

National Institute of Cardiovascular Diseases, Slovakia

Other

Collaborators

  • Central Slovakia Institute of Cardiovascular Diseases in Banská Bystrica, Slovakia
  • East Slovakia Institute of Cardiovascular Diseases in Košice, Slovakia

Registry information

Official study title

Long-term Effect of Different Modes of Endovascular Therapy in Combination With Anticoagulation Treatment in Patients With Acute Extensive Deep Vein Thrombosis (LEVANTE Research)

Acronym: LEVANTE

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Apr 24, 2023
Registry last updated
Apr 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.