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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04698902
Other study ID # 20/599-E
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2020
Est. completion date May 1, 2022

Study information

Verified date March 2024
Source Fundacion Investigacion Interhospitalaria Cardiovascular
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Calcified coronary artery disease is a frequently encountered problem that can lead to poorer outcomes for patients undergoing PCI. Recently, intravascular lithotripsy has become available for the treatment of callcified coronary artery disease. The effect of intravascular lithotripsy on varying calcium patterns has not been adequately explored. This is an investigator initiated, open label, non-blinded, observational study involving a number of centers in Spain examining the effect of intravasuclar lithotripsy in varying calcium patterns. 100 patients wll be enrolled. Optical coherence tomography will be used to assess the effect of intravascular lithotripsy on varying calcium patterns (concentric, eccentric and nodular).


Description:

Calcified coronary artery disease continues to present a challenge for Interventional Cardiologists. Moderate calcification is found in over 25% of coronary artery lesions planned for percutaneous coronary intervention (PCI). Outcomes for patients undergoing PCI to calcified lesions have been shown to be consistently poorer than in non-calcified lesions. Recently, intravascular lithotripsy has become available for the treatment of calcified coronary artery disease. The effect of intravascular lithotripsy on varying calcium patterns has not been adequately explored. This is an investigator initiated, open label, non-blinded, observational study involving a number of centers in Spain. Patients with an indication of PCI and with a significant calcium burden requiring modification will be invited to participate. PCI procedures will be performed via either radial or femoral access as deemed appropriate by the operator and in accordance with local protocols. Intravascular imaging using OCT will be performed prior to calcium modification to define the pattern of calcium, after calcium modification to assess the effectiveness of IVL therapy and after stent implantation to assess stent expansion.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date May 1, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients >18 years of age - Patients with an indication for PCI (ischemic symptoms or evidence of myocardial ischemia (inducible or spontaneous) in the presence of >50% de novo severely calcified coronary stenosis that requires IVL treatment. Exclusion Criteria: - Patients unwilling or unable to sign informed consent for the procedure - Patients with severe peripheral vascular disease limiting vascular access to the extent that it is unsafe to perform the procedure - Patients with severe renal dysfunction (eGFR <15mls/min and not receiving dialysis) - Treatment of vessels < 2.5mm diameter which are not amenable to IVL treatment or OCT assessment. - Treatment of lesions located very distally in the coronary vessel where the OCT catheter may not reach. - Inability to cross the lesion with the OCT catheter due to very severe stenosis or severe vessel tortuosity. - Ostial left main stem or right coronary artery lesions which may be difficult to visualise by OCT - Patients requiring concomitant use of rotational or orbital atherectomy of LASER.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Intracoronary lithotripsy
Intracoronary lithotripsy involves the use of sonic pressure waves generated from emitters enclosed within a balloon delivery system. The generated sonic waves act to fracture calcium within the coronary artery wall.

Locations

Country Name City State
Spain Hospital Clínico San Carlos Madrid

Sponsors (1)

Lead Sponsor Collaborator
Fundacion Investigacion Interhospitalaria Cardiovascular

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of lesions with Calcium Fractures Percentage of lesions showing calcium modification (fractures) after intravascular lithotripsy (IVL) in nodular eccentric and concentric calcium patterns At the time of percutaneous coronary intervention
Secondary Number of calcium fractures Number of calcium fractures visible on OCT after IVL treatment At the time of percutaneous coronary intervention
Secondary Number of quadrants with calcium fractures Number of quadrants with calcium fractures after IVL treatment as assessed by OCT At the time of percutaneous coronary intervention
Secondary Calcium modification in eccentric versus concentric calcium Percentage of lesions with calcium arc <180 versus >180 degrees with fractures as assessed by OCT At the time of percutaneous coronary intervention
Secondary Stent expansion Percentage stent expansion in patients with and without calcium modification (fractures) after application of IVL At the time of percutaneous coronary intervention
Secondary Stent symmetry Stent symmetry index in patients with and without calcium modification (fractures) after IVL application At the time of percutaneous coronary intervention
Secondary Stent symmetry Stent symmetry index in patients with concentric versus eccentric calcification At the time of percutaneous coronary intervention
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