MedPath

CAlcified Lesion Intervention Planning Steered by OCT.

Not Applicable
Conditions
Angioplasty
Coronary Artery Calcification
Interventions
Procedure: angioplasty
Registration Number
NCT05301218
Lead Sponsor
Institut Mutualiste Montsouris
Brief Summary

Calcified lesions are very frequent among coronary artery disease stenotic lesions.

The prevalence of calcifications ranges from 30 to 40% (by angiography evaluation) but is higher when analyzed by intra coronary imaging.

Calcified lesions are very frequent among coronary artery disease stenotic lesions. The prevalence of calcifications ranges from 30 to 40% (by angiography evaluation) but is higher when analyzed by intra coronary imaging.

The presence of calcifications increases the risk of adverse evolution after PCI , including stent restenosis, thrombosis and need for repeat revascularisation. Specific and appropriate tools can be used for calcified lesions management , including high pressure non compliant balloons, intravascular lithotripsy and rotablator. Intra vascular OCT has a high sensitivity and specificity for calcium detection among coronary artery lesions. Compared to IVUS, OCT allows a better quantification of calcium sheets (depth extension ) . Several intra coronary imaging based calcified lesions management algorithms have been proposed , but none have been validated in clinical practice.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
140
Inclusion Criteria
  1. Patient with chronic coronary syndrome

  2. Angiographically moderately to severely calcified target lesion, defined as follows:

    • Moderate: lesion with radio-opacities noted only during the cardiac cycle before contrast dye injection (Aksoy et al., Circ Cardiovasc Interv 2019)
    • Severe: lesion with radio-opacities seen without cardiac motion before contrast dye injection, visible on both sides of the arterial lumen(Aksoy et al., Circ Cardiovasc Interv 2019)
  3. Possibility to cross the target lesion with OCT catheter

Exclusion Criteria
  1. On-going cardiogenic shock
  2. Acute coronary syndrome related to target lesion
  3. Severe renal failure (Creatinine clearance: 30 ml/min/m2)
  4. Impossibility to cross target lesion with OCT catheter & balloons,
  5. Indication for Rotablator device as first line therapy
  6. Pregnancy
  7. Age < 18 y
  8. Denial to provide consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
OCT-guided groupangioplastya preliminary OCT run will be recorded. An initial predilation with 1.5 to 2.0 mm balloon could be accepted in order to facilitate OCT catheter delivery through the target lesion. The PCI strategy will be guided by a pre-defined algorithm based on initial OCT findings. Post PCI result will be assessed by control OCT and potential optimization steps could be applied according to the results. The MLD-MAX optimization approach will be applied. Final OCT run will be performed at the end of the procedure.
angiography-guided groupangioplastythe treatment (including lesion preparation, stent sizing and post implantation optimization) will be performed by angiography. Once the result is considered optimal by the operator, a control OCT run will be acquired.
Primary Outcome Measures
NameTimeMethod
The primary endpoint of the CALIPSO study is the minimal stent area (MSA) on the final OCT runDuring the procedure

The crude minimal stent area (MSA) will be measured along the stent on the target lesion. Stent geometric expansion will be evaluated by the DOCTORS criteria for non-bifurcated segments (Meneveau et, Circulation 2016) and LEMON criteria for bifurcated segments (Amabile et al;, Eurointervention 2020).

Secondary Outcome Measures
NameTimeMethod
Geometrical stent expansion (%) according to the DOCTORS or LEMON criteriaduring procedure

After the stent is deployed, the blood flow dynamics influence the mechanics by compressing and expanding the structure.

Residual post PCI (Percutaneous Coronary Intervention)stenosis (assessed by QCA methods)during procedure

Qualitative Comparative Analysis (QCA) is a methodology that enables the analysis of multiple cases in complex situations

Coronary artery perforation: incidenceduring the procedure and During the full participation period (1 year).]

Coronary perforation was defined as evidence of extravasation of dye or blood from the coronary artery during or following the interventional procedure

Major adverse cardiovascular events at 30 days and 1 yearat 30 days and 1 year

Cardiovascular death + Any myocardial infarction + need for re-intervention on the target lesion (TLR)

Radiation doseduring procedure

Differences in dose radiation used during le procedure

Total Contrast medium volumeduring procedure

Differences in amount of contrast drug used during le procedure

Procedure duration24th post-operative hour

differences in duration (time) of the procedure

Residual major struts malapposition: crude incidence and quantificationduring procedure

malapposition was defined as a lack of contact of at least 1 strut with the underlying vessel wall (at least 150 μm, in the absence of a side branch) with evidence of blood flow behind the strut. It was classified as "major" malapposition if there was evidence of at least 30% of the struts in one frame.

Peri-procedural MI according to the SCAI definition (23)during procedure

according to the SCAI definition (Moussa et al., Journal of the American College of Cardiology 2013)

Trial Locations

Locations (14)

Ch de Bastia

🇫🇷

Bastia, France

Institut Mutualiste montsouris

🇫🇷

Paris, Ile De France, France

CHU de Besançon

🇫🇷

Besançon, France

CHU de Bordeaux

🇫🇷

Bordeaux, France

CHU de Clermont-Ferrand

🇫🇷

Clermont-Ferrand, France

Clinique Saint Augustin

🇫🇷

Bordeaux, France

Hôpital Louis Pasteur

🇫🇷

Le Coudray, France

Polyclinique les Fleurs

🇫🇷

Ollioules, France

CHU Nîmes

🇫🇷

Nîmes, France

CHU de Poitiers

🇫🇷

Poitiers, France

L'Hôpital Privé du Confluent

🇫🇷

Nantes, France

Clinique Saint-Hilaire

🇫🇷

Rouen, France

Clinique Pasteur

🇫🇷

Toulouse, France

Institut Arnaud Tzanck,

🇫🇷

Saint-Laurent-du-Var, France

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