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Ultrasound-facilitated, Catheter-directed, Thrombolysis in Intermediate-high Risk Pulmonary Embolism

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NCT04790370

Sponsored by Boston Scientific Corporation (industry) · BSX — their whole pipeline →. With National PERT Consortium, Inc., University Medical Center Mainz.

Phase
Phase 4
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
544actual
Sites
60
Countries
Austria, France, Germany +6

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-08-02actualWhen the study began enrolling
Primary completion2025-07-31actualThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2026estimatedThe whole study's end, after follow-up
First posted2021-03-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Pulmonary Embolism

Interventions

  • Drug: Anticoagulation with heparin — also filed as heparin, LMWH, UFH, anticoag, antiplatelet
  • Device: EkoSonicTM Endovascular System — also filed as EKOS, USCDT, CDT, thrombolysis, fibrinolysis

Primary outcomes

what the primary-completion date above is the date OF
PE-related mortality
measured Within seven days of randomization
PE recurrence
measured Within seven days of randomization
Cardiorespiratory decompensation or collapse
measured Within seven days of randomization

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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