Status:
RECRUITING
Inflow Improve for Deep Vein ThrombOsis with Ultrasound AcceLerated ThrombOlysis and Venoplasty
Lead Sponsor:
IRCCS San Raffaele
Conditions:
Post-Thrombotic Syndrome of Both Legs
Eligibility:
All Genders
18-75 years
Brief Summary
Aim of the IDOLO study is to investigate clinical efficacy on ultrasound accelerated thrombolysis and venoplasty in patients with post-thrombotic syndrome secondary to chronical femoro-popliteal vein ...
Eligibility Criteria
Inclusion
- Patient admitted in Vascular Surgery Unit, San Raffaele Hospital, Milan
- Patients able to sign specific informed consent for the study.
- Proximal deep vein Thrombosis (iliac vein, common femoral vein, deep femoral vein, and femoral vein) that was objectively diagnosed with duplex imaging and/or venography ≥ 6 months prior to study screening.
- Persistent chronic deep vein Thrombosis causing restrictive flow, as confirmed by imaging, within 60 days prior to the study procedure.
- Failed a minimum of 3 consecutive months of conservative treatment (therapeutic anticoagulation and compression stockings).
- Villalta score ≥8 for the affected limb within 30 days prior to the study procedure
Exclusion
- Treated with mechanical thrombectomy within 2 weeks of the study thrombolysis procedure.
- Treated with thrombolysis drugs within 48 hours of the study thrombolytic procedure.
- Life expectancy less than (\<) 1 year.
- Body Mass Index (BMI) greater than (\>) 40 kilograms/square meter (kg/m\^2) or per Investigator's discretion participant is able tolerate the procedure and be compliant with post-procedure increased physical activity.
- No flow in popliteal vein on duplex imaging
- Thrombus extending ≥ 3 centimeters (cm) into the inferior vena cava (IVC). If central venous occlusion, consider computed tomography (CT) or magnetic resonance venography (MRV). For participants with bilateral DVT, it is recommended that central imaging be performed prior to treatment to evaluate the status of the IVC.
- Active bleeding, recent (\<3 months) gastrointestinal (GI) bleeding, active peptic ulcer, severe liver dysfunction, and bleeding diathesis.
- Recent (\<3 months) internal eye surgery or hemorrhagic retinopathy; recent (\<10 days) major surgery, cataract surgery, trauma, cardiopulmonary resuscitation (CPR), obstetrical delivery, or other invasive procedure.
- History of stroke or intracranial/intraspinal bleed, tumor, vascular malformation, or aneurysm.
- Active cancer (metastatic, progressive, or treated within the last 6 months). Participants with non-melanoma primary skin cancers are eligible to participate in the study.
- Hemoglobin \<9.0 milligrams/deciliter (mg/dL) within 24 hours prior to the procedure
- International normalized ratio (INR) ≥1.5 nanograms/deciliter (ng/dL) within 24 hours prior to the procedure.
- Platelet count \<100,000 cells/cubic millimeter (cells/mm\^3) or \>700,000 cells/mm\^3 within 24 hours prior to the procedure.
- Creatinine outside the normal range for the treating institution and considered clinically significant by the Investigator.
- Uncontrolled hypertension, defined as systolic \>175 millimeters of mercury (mmHg) and a diastolic \>110 mmHg.
- Use of clopidogrel, ticlopidine, or other thienopyridine antiplatelet drug within 7 days of the study procedure.
- In the judgment of the clinician, the participant is at high risk for catastrophic bleeding.
- Impossibility or refusal to give informed consent
Key Trial Info
Start Date :
January 29 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 15 2027
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06198816
Start Date
January 29 2024
End Date
January 15 2027
Last Update
March 24 2025
Active Locations (1)
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1
San Raffaele Hospital
Milan, Italy, Italy, 20132