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Dissecting the Role of Distal Embolization of Athero-thrombotic Material in Primary PCI: the ThrombOticBurden and mIcrovAscularobStruction (TOBIAS) Study.

Phase 4
Conditions
Acute Myocardial Infarction
Interventions
Device: angio-guided thrombus aspiration (Eliminate catheter, Terumo, Tokyo, Japan)
Device: OCT-guided thrombus aspiration (Eliminate catheter, Terumo, Tokyo, Japan)
Registration Number
NCT01914055
Lead Sponsor
Ospedale San Donato
Brief Summary

demonstrate that FD-OCT guidance is feasible and possibly results in reduction of frequency-domain Optical Coherence Tomography-defined residual thrombus burden after thrombus-aspiration.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • ST elevation myocardial infarction
  • Ages Eligible for Study: >18 years old
  • Genders Eligible for Study: Both (female sex with child-bearing potential excluded)
Exclusion Criteria
  • occluded (TIMI 0) or sub occluded (TIMI 1) proximal vessel of estimated diameter ≥3mm
  • intended use of thrombus aspiration

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
angio-guided thrombus aspirationangio-guided thrombus aspiration (Eliminate catheter, Terumo, Tokyo, Japan)thrombus aspiration guided by angiography
OCT-guided thrombus aspirationOCT-guided thrombus aspiration (Eliminate catheter, Terumo, Tokyo, Japan)thrombus aspiration guided by optical coherence tomography
Primary Outcome Measures
NameTimeMethod
number of cross-sections with thrombus area more than 10% at post-stenting frequency-domain (FD) Optical Coherence Tomographywithin the primary PCI procedure

Whether FD-OCT guidance of manual thrombus aspiration (TA) is superior to conventional angio-guided TA in reducing residual thrombus burden after stenting (defined as the number of cross-sections with thrombus area more than 10% at post-stenting FD-OCT)

Secondary Outcome Measures
NameTimeMethod
major adverse cardiac eventsat 6 months

rate of major adverse cardiac events at 6 months from the index procedure

Trial Locations

Locations (1)

Cardiovascular Department, Ospedale S.Donato

🇮🇹

Arezzo, AR, Italy

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