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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02502851
Other study ID # SK 108 -- 120/14
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2014
Est. completion date October 2019

Study information

Verified date March 2020
Source Segeberger Kliniken GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to evaluate the success of lesion preparation with either rotational atherectomy or cutting/scoring balloons as well as the long term effects of a hybrid sirolimus-eluting stent in an angiographically well-defined group of patients with complex calcified coronary lesions.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date October 2019
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Clinical inclusion criteria

- Age above 18 years and consentable

- Angiographically proven coronary artery disease

- Anginal symptoms and/or reproducible ischemia in the target area by ECG, functional stress testing or fractional flow reserve

- Written informed consent

2. Angiographic inclusion criteria

- De-novo lesion in a native coronary artery

- Target reference vessel diameter between 2.25 and 4.0 mm by visual estimation

- Luminal diameter reduction of 50-100% by visual estimation

- Severe calcification of the target lesion

Exclusion Criteria:

1. Clinical exclusion criteria

- Myocardial infarction (within 1 week)

- Decompensated heart failure

- Limited long term prognosis due to other conditions

2. Angiographic exclusion criteria

- Target lesion is in a coronary artery bypass graft

- Target lesion is an in-stent restenosis

- Target vessel thrombus

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Rotational Atherectomy
Calcified lesion preparation using rotational atherectomy before implantation of the Orsiro drug eluting stent
Cutting/Scoring Balloon
Calcified lesion preparation using cutting/scoring balloons before implantation of the Orsiro drug eluting stent

Locations

Country Name City State
Germany Segeberger Kliniken GmbH Bad Segeberg Schleswig-Holstein

Sponsors (1)

Lead Sponsor Collaborator
Segeberger Kliniken GmbH

Country where clinical trial is conducted

Germany, 

References & Publications (10)

Abdel-Wahab M, Richardt G, Joachim Büttner H, Toelg R, Geist V, Meinertz T, Schofer J, King L, Neumann FJ, Khattab AA. High-speed rotational atherectomy before paclitaxel-eluting stent implantation in complex calcified coronary lesions: the randomized ROTAXUS (Rotational Atherectomy Prior to Taxus Stent Treatment for Complex Native Coronary Artery Disease) trial. JACC Cardiovasc Interv. 2013 Jan;6(1):10-9. doi: 10.1016/j.jcin.2012.07.017. Epub 2012 Dec 19. — View Citation

Fonseca A, Costa Jde R Jr, Abizaid A, Feres F, Abizaid AS, Costa R, Staico R, Mattos LA, Sousa AG, Grube E, Sousa JE. Intravascular ultrasound assessment of the novel AngioSculpt scoring balloon catheter for the treatment of complex coronary lesions. J Invasive Cardiol. 2008 Jan;20(1):21-7. — View Citation

Hamon M, Niculescu R, Deleanu D, Dorobantu M, Weissman NJ, Waksman R. Clinical and angiographic experience with a third-generation drug-eluting Orsiro stent in the treatment of single de novo coronary artery lesions (BIOFLOW-I): a prospective, first-in-man study. EuroIntervention. 2013 Jan 22;8(9):1006-11. doi: 10.4244/EIJV8I9A155. — View Citation

Kawaguchi R, Tsurugaya H, Hoshizaki H, Toyama T, Oshima S, Taniguchi K. Impact of lesion calcification on clinical and angiographic outcome after sirolimus-eluting stent implantation in real-world patients. Cardiovasc Revasc Med. 2008 Jan-Mar;9(1):2-8. doi: 10.1016/j.carrev.2007.07.004. — View Citation

Kawamori H, Shite J, Shinke T, Otake H, Matsumoto D, Nakagawa M, Nagoshi R, Kozuki A, Hariki H, Inoue T, Osue T, Taniguchi Y, Nishio R, Hiranuma N, Hirata K. Natural consequence of post-intervention stent malapposition, thrombus, tissue prolapse, and dissection assessed by optical coherence tomography at mid-term follow-up. Eur Heart J Cardiovasc Imaging. 2013 Sep;14(9):865-75. doi: 10.1093/ehjci/jes299. Epub 2013 Jan 4. — View Citation

Kuriyama N, Kobayashi Y, Yamaguchi M, Shibata Y. Usefulness of rotational atherectomy in preventing polymer damage of everolimus-eluting stent in calcified coronary artery. JACC Cardiovasc Interv. 2011 May;4(5):588-9. doi: 10.1016/j.jcin.2010.11.017. — View Citation

Madhavan MV, Tarigopula M, Mintz GS, Maehara A, Stone GW, Généreux P. Coronary artery calcification: pathogenesis and prognostic implications. J Am Coll Cardiol. 2014 May 6;63(17):1703-14. doi: 10.1016/j.jacc.2014.01.017. Epub 2014 Feb 12. Review. — View Citation

Mooney M, Teirstein P, Moses J, Turco M, Reisman M, Waksman R, Saucedo J, Mauri L, Lee D, Gershony G, Mehran R, Carlier S, Lansky A, Leon M. Final Results from the U.S. Multi-Center Trial of the AngioSculpt Scoring Balloon Catheter for the Treatment of Complex Coronary Artery Lesions. Am J Cardiol 2006;98:121.

Prati F, Regar E, Mintz GS, Arbustini E, Di Mario C, Jang IK, Akasaka T, Costa M, Guagliumi G, Grube E, Ozaki Y, Pinto F, Serruys PW; Expert's OCT Review Document. Expert review document on methodology, terminology, and clinical applications of optical coherence tomography: physical principles, methodology of image acquisition, and clinical application for assessment of coronary arteries and atherosclerosis. Eur Heart J. 2010 Feb;31(4):401-15. doi: 10.1093/eurheartj/ehp433. Epub 2009 Nov 4. Review. — View Citation

Vaquerizo B, Serra A, Miranda F, Triano JL, Sierra G, Delgado G, Puentes A, Mojal S, Brugera J. Aggressive plaque modification with rotational atherectomy and/or cutting balloon before drug-eluting stent implantation for the treatment of calcified coronary lesions. J Interv Cardiol. 2010 Jun;23(3):240-8. doi: 10.1111/j.1540-8183.2010.00547.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Strategy Success The primary endpoint will be 'Strategy Success' defined as successful stent delivery and expansion with attainment of < 20% in-stent residual stenosis of the target lesion in the presence of TIMI 3 flow without crossover or stent failure Intraprocedural
Primary In-Stent late lumen loss at 9 months Co-primary Endpoint: The in-stent late lumen loss at 9 months, defined as the difference between the postprocedure in-stent minimal lumen diameter (MLD) and the in-stent MLD at 9-month followup angiography. 9 months
Secondary Target vessel failure (TVF) Target vessel failure (TVF) defined as a composite of cardiac death, target vessel related myocardial infarction (MI; Q- or non-Q-wave) and clinically driven target vessel revascularization (TVR) at 9 months, 1 and 2 years 9 months, 1 year, 2 years
Secondary In-segment late lumen loss at 9 months In-segment late lumen loss (stent length + 5 mm on either side) at 9 months 9 months
Secondary In-segment binary restenosis at 9 months In-segment binary restenosis (diameter stenosis = 50%) at 9 months 9 months
Secondary Stent thrombosis at 9 months, 1 and 2 years Stent thrombosis at 9 months, 1 and 2 years 9 months, 1 and 2 years
Secondary Peri-procedural MI within 72 hrs
Secondary Procedural duration Intraproedural
Secondary Amount of contrast dye Intraprocedural