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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04298307
Other study ID # EPIC18-REPLICA
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 4, 2020
Est. completion date November 1, 2024

Study information

Verified date July 2022
Source Fundación EPIC
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The REPLICA TRIAL tries to assess the intracoronary lithotripsy safety and efficacy profiles in real-world patients with calcified coronary artery disease.


Description:

The REPLICA TRIAL tries to assess the intracoronary lithotripsy safety and efficacy profiles in real-world patients with calcified coronary artery disease requiring percutaneous revascularization with stent implantation.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 400
Est. completion date November 1, 2024
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients = 18 years of age. - Patients with calcified coronary artery disease requiring percutaneous revascularization with stent implantation who, at the operator's discretion and according to the hospital routine clinical practice, require an ICL with the Shockwave catheter. - The patients have been informed of the study characteristics and have given their written informed consent. Exclusion Criteria: - Refusal to participate in this study. - Patients whose life expectancy is < 1 year. - Patients with hemodynamic instability with Killip class III or IV.

Study Design


Intervention

Other:
Intracoronary lithotripsy (ICL)
ICL using the Shockwave catheter.

Locations

Country Name City State
Spain Hospital Universitario A Coruña A Coruña LA Coruña
Spain Hospital General Universitario de Albacete Albacete
Spain Hospital Universitario de Badajoz Badajoz
Spain Hospital Universitari Germans Trias I Pujol Badalona Barcelona
Spain Hospital General Universitario de Ciudad Real Ciudad Real
Spain Hospital Universitario de Cabueñes Gijón Asturias
Spain Hospital Universitari de Bellvitge Hospitalet de Llobregat Barcelona
Spain Hospital de León León
Spain Hospital Universitario Lucus Agusti Lugo
Spain Hospital Central de La Defensa Madrid
Spain Hospital Clinico San Carlos Madrid
Spain Hospital La Luz Madrid
Spain Hospital Universitario La Paz Madrid
Spain Hospital Universitario La Princesa Madrid
Spain Hospital Universitario Puerta de Hierro Majadahonda
Spain Hospital Universitario Central de Asturias Oviedo Asturias
Spain Hospital Universitario de Salamanca Salamanca
Spain Hospital Universitario Donostia San Sebastián
Spain Hospital Universitario Marques de Valdecilla Santander Cantabria
Spain Hospital Clinico Universitario de Santiago de Compostela Santiago De Compostela Coruña
Spain Hospital Universitari Joan Xxiii Tarragona
Spain Hospital Universitario Mutua de Terrassa Terrassa Barcelona
Spain Hospital Universitario Virgen de La Salud de Toledo Toledo
Spain Hospital Clinico Universitario de Valladolid Valladolid
Spain Hospital Universitario Alvaro Cunqueiro Vigo Pontevedra
Spain Hospital Universitario Miquel Servet Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
Fundación EPIC

Country where clinical trial is conducted

Spain, 

References & Publications (5)

Ali ZA, Nef H, Escaned J, Werner N, Banning AP, Hill JM, De Bruyne B, Montorfano M, Lefevre T, Stone GW, Crowley A, Matsumura M, Maehara A, Lansky AJ, Fajadet J, Di Mario C. Safety and Effectiveness of Coronary Intravascular Lithotripsy for Treatment of Severely Calcified Coronary Stenoses: The Disrupt CAD II Study. Circ Cardiovasc Interv. 2019 Oct;12(10):e008434. doi: 10.1161/CIRCINTERVENTIONS.119.008434. Epub 2019 Sep 25. — View Citation

Bourantas CV, Zhang YJ, Garg S, Iqbal J, Valgimigli M, Windecker S, Mohr FW, Silber S, Vries Td, Onuma Y, Garcia-Garcia HM, Morel MA, Serruys PW. Prognostic implications of coronary calcification in patients with obstructive coronary artery disease treated by percutaneous coronary intervention: a patient-level pooled analysis of 7 contemporary stent trials. Heart. 2014 Aug;100(15):1158-64. doi: 10.1136/heartjnl-2013-305180. Epub 2014 May 20. — View Citation

Brinton TJ, Ali ZA, Hill JM, Meredith IT, Maehara A, Illindala U, Lansky A, Götberg M, Van Mieghem NM, Whitbourn R, Fajadet J, Di Mario C. Feasibility of Shockwave Coronary Intravascular Lithotripsy for the Treatment of Calcified Coronary Stenoses. Circulation. 2019 Feb 5;139(6):834-836. doi: 10.1161/CIRCULATIONAHA.118.036531. — View Citation

Vilalta V, Rodriguez-Leor O, Cid-Alvarez B, et al. Intracoronary Lithotripsy in a High-risk Real-world Population: First Experience in Severely Calcified, Complex Coronary Lesions. REC Interv Cardiol 2019; in press.

Wong B, El-Jack S, Newcombe R, Glenie T, Armstrong G, Khan A. Shockwave Intravascular Lithotripsy for Calcified Coronary Lesions: First Real-World Experience. J Invasive Cardiol. 2019 Mar;31(3):46-48. Epub 2019 Feb 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Procedural success Assessment of procedural success defined as angiographic results (TIMI grade 3 and residual stenosis < 20% without in-hospital complications ). Index Procedure
Secondary MACE Major Cardiovascular Adverse Events (MACE), defined as a composite of cardiac death, target vessel related nonfatal infarction or need for unplanned target vessel revascularization during hospital admission. Index Procedure
Secondary MACE Major Cardiovascular Adverse Events (MACE), defined as a composite of cardiac death, target vessel related nonfatal infarction or need for unplanned target vessel revascularization. 12 months
Secondary Residual stenosis Assessment of angiographic stenosis during stent implantation Index Procedure
Secondary Death (all cause) Death (all cause) 12 months
Secondary Death (cardiovascular) Death (cardiovascular) 12 months
Secondary Non-fatal Myocardial Infarction Non-fatal Myocardial Infarction 12 months
Secondary Target Vessel Revascularization Target Vessel Revascularization 12 months
Secondary Stent thrombosis of target lesion Stent thrombosis of target lesion 12 months
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