Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dilatation
NCT ID: NCT06558474
Last Updated: 2025-08-07
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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RECRUITING
12000 participants
OBSERVATIONAL
2023-09-01
2026-05-01
Brief Summary
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Post-dilation is often performed to achieve optimal stent expansion and reduce stent malapposition of stent struts, aiming to reduce stent thrombosis and restenosis both short term as long term. However, there are limited studies that have explored the effect of post-dilatation for stent optimization on clinical outcomes. As a result of the restricted evidence, there is no consensus whether post-dilatation should be used routinely in clinical practice and the extent to which post-dilatation is being utilized remains unclear.
For this reason, the OPTIMIZE PCI was designed, a national registry-based quality improvement project to implement a liberal post-dilatation strategy in multiple PCI centers in the Netherlands. As part of the OPTIMIZE-PCI, a retrospective observational analysis will eventually be conducted to evaluate whether adopting this strategy has led to improved clinical outcomes after PCI in terms of major adverse cardiac events.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pre-intervention/implementation cohort
In the first phase, data additional to the national PCI registry will be analyzed retrospectively from all patients receiving PCI from January 2021 to January 2022. Data on the percentage of use of post-dilatation using high-pressure non-compliant (HPNC) balloon by the individual interventional cardiologist will be collected. This will establish a benchmark from which individual interventional cardiologists must increase their use of post-dilatation.
No interventions assigned to this group
Post-intervention/implementation cohort
During this implementation phase, all individual PCI operators of the participating centres will be informed to liberally use post-dilatation for stent optimization during PCI. Operators are requested to increase their use of post-dilatation with at least 20% or use post-diltation in at least 85% of the PCI's. Throughout the project, individual participating operators will receive individual feedback on the percentage use of post-dilatation with prospective data collection after 2, 4, 6, 9 and 12 months. Based on this result, the implementation process will be refined as necessary. The duration of this phase will be approximately 1 year per centre.
Eventually a retrospective observational anlaysis, comparing the two cohorts, will be conducted to evaluate whether adopting this strategy has led to improved clinical outcomes after PCI in terms of major adverse cardiac events.
Liberal post-dilatation strategy during PCI
A liberal post-dilatation strategy for stent optimization during PCI will be implemented in multiple centers in the Netherlands.
This include an increase of post-dilatation use of at least 20% per operator, or a percentage of post-dilatation of at least 85%.
Operators will be asked to enforce a very low threshold for post-dilatation in general, with a mandatory HPNC post-dilatation for the following indications:
* In case of any calcification
* Delta of ≥ 0.5mm between the distal and proximal reference diameter of the treated coronary segment
* Stent length \>24 mm
* Signs of incomplete stentframe-deployment on angiography or StentBoost
* In case of CTO
* In case of bifurcation PCI (Left main and non-left main)
* Proximal Optimisation Technique (POT) with NC balloon
* Final Kissing Balloon dilatation (FKB) with preferentially first sequential high-pressure inflations and final low pressure kiss both with NC balloons
Interventions
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Liberal post-dilatation strategy during PCI
A liberal post-dilatation strategy for stent optimization during PCI will be implemented in multiple centers in the Netherlands.
This include an increase of post-dilatation use of at least 20% per operator, or a percentage of post-dilatation of at least 85%.
Operators will be asked to enforce a very low threshold for post-dilatation in general, with a mandatory HPNC post-dilatation for the following indications:
* In case of any calcification
* Delta of ≥ 0.5mm between the distal and proximal reference diameter of the treated coronary segment
* Stent length \>24 mm
* Signs of incomplete stentframe-deployment on angiography or StentBoost
* In case of CTO
* In case of bifurcation PCI (Left main and non-left main)
* Proximal Optimisation Technique (POT) with NC balloon
* Final Kissing Balloon dilatation (FKB) with preferentially first sequential high-pressure inflations and final low pressure kiss both with NC balloons
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Medtronic
INDUSTRY
Cathreine BV
OTHER
Responsible Party
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Koen Teeuwen
Principal investigator
Locations
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Catharina Hospital
Eindhoven, North Brabant, Netherlands
Countries
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Central Contacts
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Facility Contacts
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Koen Teeuwen, MD, PhD
Role: primary
References
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van Beek KAJ, Timmermans MJC, Derks L, Cheng JM, Kraaijeveld AO, Arkenbout EK, Schotborgh CE, Brouwer J, Claessen BE, Lipsic E, Polad J, van Nunen LX, Sjauw K, van Veghel D, Tonino PA, Teeuwen K; 'on behalf of the PCI registration committee of The Netherlands Heart Registration'. Contemporary Use of Post-Dilatation for Stent Optimization During Percutaneous Coronary Intervention; Results From the Netherlands Heart Registration. Catheter Cardiovasc Interv. 2025 Mar;105(4):870-877. doi: 10.1002/ccd.31404. Epub 2025 Jan 8.
Slingerland SR, van Beek KAJ, Schulz DN, van Steenbergen GJ, Brouwer T, Stoel M, Vlaar PJ, Tonino PA, Dekker L, van Nunen LX, Teeuwen K, van Veghel D. Results of systematic patient outcome monitoring: Does post-dilatation during angiography-guided percutaneous coronary intervention improve clinical outcomes? Hellenic J Cardiol. 2025 Mar-Apr;82:26-33. doi: 10.1016/j.hjc.2023.11.004. Epub 2023 Nov 16.
Other Identifiers
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CathreineBV
Identifier Type: -
Identifier Source: org_study_id
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