Mechanical Thrombectomy for Acute Pulmonary Embolism

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-75
SponsorRenJi Hospital

About this trial

Research Objective:

To prospectively compare the efficacy and safety of a pre-collaboratively developed ultra-thin PTFE minimally invasive thrombectomy system versus standard pharmacological therapy in patients with acute pulmonary embolism (PE), both administered on top of standard care.

Research Content:

Patients meeting all the following criteria will be enrolled:

Aged 18-75 years (male or female)

Clinically diagnosed with acute PE

Right ventricular/left ventricular diameter ratio (RV/LV) ≥0.9 on computed tomographic pulmonary angiography (CTPA)

Provision of voluntary written informed consent.

Study Design:

After confirming eligibility, subjects will be randomized at a 1:1 ratio into two groups:

Innovative Device Group: Minimally invasive thrombectomy

Standard Pharmacological Therapy Group: Pharmacological thrombolysis + anticoagulation

Study Endpoints:

Primary Efficacy Endpoint:

Reduction in RV/LV ratio (measured by CTPA) from baseline to 48 hours post-treatment.

Primary Safety Endpoint:

Incidence of Major Adverse Events (MAEs) from baseline to 48 hours post-treatment, defined as:

Procedure-related death

Major bleeding (per VARC-2 criteria: life-threatening, disabling, or major bleeding)

Treatment-related clinical deterioration, including:

Unplanned mechanical ventilation

Arterial hypotension (systolic blood pressure \<90 mmHg for \>1 hour or requiring vasopressors) or shock

Cardiopulmonary resuscitation

Sustained deterioration in oxygenation

Emergency surgical embolectomy.

Key Terminology Notes:

RV/LV: Right Ventricular/Left Ventricular diameter ratio (standard medical abbreviation retained).

VARC-2: Valve Academic Research Consortium-2 (internationally recognized bleeding criteria).

PTFE: Polytetrafluoroethylene (material name preserved).

MAE: Major Adverse Events (acronym defined at first use).

Clinical deterioration: Explicitly specified with objective clinical indicators.

This translation maintains scientific precision while adhering to international clinical trial reporting standards (ICH-GCP). The structure aligns with typical English-language study protocols for clarity and reproducibility.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18-75 years (male or female)

Clinically diagnosed with acute PE

Right ventricular/left ventricular diameter ratio (RV/LV) ≥0.9 on computed tomographic pulmonary angiography (CTPA)

Provision of voluntary written informed consent.

Disqualifiers

Target vessel diameter <6 mm

Calcification, plaque, or stenosis in target lesion

Sustained systolic blood pressure <90 mmHg for >15 minutes or requiring vasopressors to maintain SBP ≥90 mmHg

Peak pulmonary artery pressure >70 mmHg

Trial design

Design model

Parallel

Treatments tested in this trial

  • Innovative Device Group

    Procedure/Surgery

    Catheter-based thrombectomy is performed within 4 hours after baseline CTPA acquisition. Pre-procedural anticoagulation with either low-molecular-weight heparin (LMWH) or unfractionated heparin (UFH) is administered prior to thrombectomy. Post-procedural oral anticoagulation is transitioned to rivaroxaban 20 mg once daily (QD).

  • Standard Pharmacological Therapy Group

    Drug

    Following thrombolytic agent administration, anticoagulation with rivaroxaban is initiated and maintained at 15 mg twice daily (BID) for the initial 3 weeks, then switched to 20 mg once daily (QD) thereafter.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Innovative Device Group: Minimally invasive thrombectomyExperimental treatment 1 intervention
Group B: Standard Pharmacological Therapy Group: Pharmacological thrombolysis + anticoagulationActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Primary Efficacy Endpoint

Reduction in RV/LV ratio (measured by CTPA) from baseline to 48 hours post-treatment.

Time frame
48 hours post-treatment.
2

Primary Safety Endpoint:

Incidence of Major Adverse Events (MAEs) from baseline to 48 hours post-treatment

Time frame
48 hours post-treatment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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