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Active, Not Recruiting

NCT Number: NCT05493904

PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment of COMPLEX Lesion (PRECISION-COMPLEX)

The aim of the study is to compare post-interventional fractional flow reserve (FFR) value between optical coherence tomography(OCT)-guided and angiography-guided strategy for treatment of complex coronary lesion.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chonnam National University Hospital, Gwangju, South Korea

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About this study

There has been ample evidence of the role of intracoronary imaging for optimizing the stent, especially among the patients with complex coronary lesions. Intracoronary imaging can be used during the entire process of percutaneous coronary intervention (PCI), from pre-PCI to post-PCI stages. Notably, approximately 15-20% of patients who underwent angiographically successful PCI showed significant stent underexpansion, malapposition, intra-stent thrombus formation, and edge dissection on intracoronary imaging studies, including optical coherence tomography (OCT).

Meanwhile, the role of pre-interventional fractional flow reserve (FFR) measurement has been well established and recommended by recent guideline. However, although previous studies evaluated the efficacy and safety of FFR-guided decision-making followed by angiographic stent implantation, they did not evaluate functionally optimized revascularization. Actually, the vessels with low post-PCI FFR had substantial proportions of suboptimized stented (underexpansion and acute malapposition) and residual disease in non-stented segments. Furthermore, several large observational studies have suggested that suboptimal physiologic results after PCI is associated with an increased risk of clinical events. Previously, the DOCTORS trial found out that OCT-guided PCI was associated with higher post-PCI FFR than angiography-guided PCI (0.94±0.04 vs. 0.92±0.05, P=0.005).

Therefore, OCT can be a useful tool for acquiring functional optimal results after stent implantation. This synergic effect between OCT and post-PCI FFR can be maximized when the investigators perform PCI for complex lesions. This study sought to evaluate compare post-interventional FFR value between OCT-guided and angiography-guided strategy for treatment of complex coronary lesion.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients >18 years old
  • Patients with stable or unstable angina and complex coronary lesions*
  • Patients who were indicated revascularization
  • Diameter stenosis >90% by angiography
  • Diameter stenosis with 50~90% with pre-interventional FFR ≤0.80
  • Patients who underwent implantation of 2nd generation drug-eluting stent
  • Definitions of complex coronary lesions
  • True bifurcation lesion (Medina 1,1,1/1,0,1/0,1,1) with side branch ≥2.5mm size
  • Chronic total occlusion (≥3 months) as target lesion
  • PCI for unprotected left main (LM) disease (LM os, body, distal LM bifurcation including non-true bifurcation)
  • Long coronary lesions (implanted stent ≥38 mm in length)
  • Multi-vessel PCI (≥2 major epicardial coronary arteries treated at one PCI session)
  • Multiple stents needed (≥3 more stent per patient)
  • In-stent restenosis lesion as target lesion
  • Severely calcified lesion (encircling calcium in angiography)
  • Left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA) ostial lesion

Exclusion criteria

  • Target lesions not amenable for PCI by operators' decision
  • Cardiogenic shock (Killip class IV) at presentation
  • Less than TIMI 3 flow of target vessel after index procedure
  • Intolerance to Aspirin, Clopidogrel, Prasugrel, Ticagrelor, Heparin, Everolimus, Zotarolimus, Biolimus, or Sirolimus
  • Known true anaphylaxis to contrast medium (not allergic reaction but anaphylactic shock)
  • Renal insufficiency such that an additional contrast medium would be harmful for patient
  • Recent ST-segment elevation myocardial infarction (STEMI)
  • Inability to receive adenosine or nicorandil injection
  • Pregnancy or breast feeding
  • Non-cardiac co-morbid conditions are present with life expectancy <2 year or that may result in protocol non-compliance (per site investigator's medical judgment)
  • Unwillingness or inability to comply with the procedures described in this protocol

Treatment and study plan

OCT-guided PCI

Procedure

For patients randomly allocated to this arm, PCI for complex lesions will be performed using OCT.

OCT Reference site: Most normal looking segment, No Lipidic plaque. Operator can decide 1 of 2 methods for stent sizing.

  • By measuring vessel diameter at the distal reference sites (in case of ≥180° of the external elastic membrane [EEL] can be identified). In this case, stent diameter will be determined using mean external elastic membrane diameter at the distal reference, rounded down to the nearest 0.25mm (Ex> mean external elastic membrane reference diameter 3.35mm, 3.25mm stent diameter will be chosen).
  • By measuring lumen diameter at the distal reference sites (in case of ≥180° of the external elastic membrane cannot be identified). In this case, stent diameter will be determined using mean lumen diameter at the distal reference, rounded up to the nearest 0.25mm (Ex> mean distal reference lumen diameter 2.55mm, 2.75mm stent diameter will be chosen).

Angiography-guided PCI

Procedure

For patients randomly allocated to this arm, PCI for complex lesions will be performed using angiography only.

The optimization guided by angiography should meet the criteria of angiographic residual diameter stenosis less than 30% by visual estimation and the absence of flow limiting dissection (≥Type C dissection). When angiographic under-expansion of the stent is suspected, adjunctive balloon dilatation will be strongly recommended.

Drug-Eluting Stent

Device

All patient will be received percutaneous coronary intervention with second generation drug-eluting stent.

Primary outcomes

  1. Suboptimal post-PCI physiological results

    Time frame: Immediate after the index procedure

    Proportion of patients with a final post-interventional fractional flow reserve <0.85

Secondary outcomes

  1. Rate of target vessel failure (TVF)

    Time frame: 2 years after last patient enrollment

    a composite of cardiac death, target-vessel myocardial infarction (MI), and target-vessel revascularization (TVR)

  2. Rate of all-cause death

    Time frame: 2 years after last patient enrollment

    death from any-cause

  3. Rate of cardiac death

    Time frame: 2 years after last patient enrollment

    death from cardiac-cause

  4. Rate of target vessel MI without periprocedural MI

    Time frame: 2 years after last patient enrollment

    Myocardial infarction without periprocedural myocardial infarction

  5. Rate of target vessel MI with periprocedural MI

    Time frame: 2 years after last patient enrollment

    Myocardial infarction with periprocedural myocardial infarction

  6. Rate of target lesion revascularization (TLR)

    Time frame: 2 years after last patient enrollment

    ischemia-driven or all

  7. Rate of target vessel revascularization (TVR)

    Time frame: 2 years after last patient enrollment

    ischemia-driven or all

  8. Rate of any MI

    Time frame: 2 years after last patient enrollment

    any myocardial infarction

  9. Rate of any revascularization

    Time frame: 2 years after last patient enrollment

    ischemia-driven or all

  10. Rate of stent thrombosis

    Time frame: 2 years after last patient enrollment

    definite, probable, or possible

  11. FFR gain between pre- and post-interventional stages

    Time frame: Immediate after the index procedure

    [Post-interventional fractional flow reserve value] - [Pre-interventional fractional flow reserve value]

  12. Trans-stent FFR gradient

    Time frame: Immediate after the index procedure

    FFR gradient across the stent (ΔFFRstent)

  13. Post-interventional non-hyperemic pressure ratios

    Time frame: Immediate after the index procedure

    Values of post-PCI non-hyperemic pressure ratios

Other outcomes

  1. Incidence of contrast-induced nephropathy

    Time frame: 48-72 hours after index procedure

    defined as an increase in serum creatinine of ≥0.5mg/dL or ≥25% from baseline after contrast agent exposure

  2. Total procedure time

    Time frame: Immediate after the index procedure

    Total procedure time

  3. Total amount of contrast dose

    Time frame: Immediate after the index procedure

    Total amount of contrast dose

  4. Total fluoroscopy time

    Time frame: Immediate after the index procedure

    Total fluoroscopy time

  5. Total amount of radiation dose

    Time frame: Immediate after the index procedure

    Total amount of radiation dose

Sponsors and collaborators

Lead sponsor

Chonnam National University Hospital

Other

Collaborators

  • Abbott Medical Devices

Registry information

Official study title

Impact of Optical Coherence Tomography-guided Versus Angiography-guided Stent Optimization on Post-Interventional Fractional Flow Reserve in Patients With Complex Coronary Artery Lesions

Important dates

Study start
2022
Primary completion
2024
Study completion
2027
First posted
Aug 9, 2022
Registry last updated
May 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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