Intravascular Identification and Drug-Eluting Balloon Treatment of Vulnerable Lipid-Rich Plaques
NCT ID: NCT04765956
Last Updated: 2023-02-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
40 participants
INTERVENTIONAL
2021-01-19
2023-09-09
Brief Summary
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Objectives: To determine the change in plaque characteristics of non-culprit LRPs, as measured with IVUS/NIRS, after treatment with DEB in patients with ACS.
Study design: Prospective single-arm clinical trial
Study population: Patients with non-ST-elevation acute coronary syndromes
Intervention: If a LRP is detected with IVUS/NIRS, it will be treated with DEB. In case multiple LRPs are detected, only one will be treated.
Main study endpoints: The difference in LCBImm4 between baseline and 9 months of plaques treated with DEB.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Drug-eluting balloon treatment
Drug-eluting balloon (DEB) treatment of lipid-rich plaque
Drug-eluting balloon treatment
Drug-eluting balloon (DEB) treatment of lipid-rich plaque
Interventions
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Drug-eluting balloon treatment
Drug-eluting balloon (DEB) treatment of lipid-rich plaque
Eligibility Criteria
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Inclusion Criteria
* An invasive revascularization strategy for NSTE-ACS with PCI is chosen.
Exclusion Criteria
2. Presence of a chronic total occlusion;
3. Too many (complex) coronary lesions requiring staged PCI procedure(s);
4. Procedural complication of the index PCI;
5. Unstable patients (the presence of cardiogenic shock, need for intubation, need for inotropes);
6. Patients with ST-segment elevations on the ECG requiring immediate primary PCI;
7. Body weight \> 250 kg;
8. Known renal insufficiency (estimated Glomerular Filtration Rate \[eGFR\] \<30 mL/min/1.73m2 or subject on dialysis);
9. Hypersensitivity or allergy to contrast with inability to properly pre-hydrate;
10. Presence of a comorbid condition with a life expectancy of less than one year;
11. Participation in another trial;
12. Subject is belonging to a vulnerable population (per investigator's judgment, e.g., subordinate hospital staff) or is unable to read or write.
ALL
No
Sponsors
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Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
OTHER
Responsible Party
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J.P.S Henriques
Prof. Dr.
Locations
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Amsterdam UMC, location AMC
Amsterdam, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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DEBuT-LRP
Identifier Type: -
Identifier Source: org_study_id
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