Rapamycin-Eluting Stents With Different Polymer Coating to Reduce Restenosis (ISAR-TEST-3)

Phase 4

Completed

• Conditions: Coronary Heart Disease
• Interventions: Device: polymer-free, rapamycin-eluting stent; Device: rapamycin-eluting stent with biodegradable polymer; Device: rapamycin-eluting Stent with permanent polymer

• Registration Number: NCT00350454
• Lead Sponsor: Deutsches Herzzentrum Muenchen

Brief Summary

The purpose of this study is to evaluate the efficacy of 3 different rapamycin-eluting-stent platforms to reduce coronary artery reblockage after stent implantation

Detailed Description

Coronary artery reblockage remains still a drawback of percutaneous coronary interventions even in the era of drug-eluting stents (DES). DESs working principle consists of the delivery of controlled amounts of antiproliferative agents at the local level, which results in the suppression of neointimal proliferation, the main cause of lumen re-narrowing after stent implantation. At present, several DES platforms have been developed and evaluated for clinical use. They differ between them with regard to the stent type, anti-proliferative drug, presence of polymers employed for drug storage and modification of drug-release kinetics as well as type of polymer used for this purpose. Although their mid-term efficacy has been well-established, there is an ongoing debate on the potential of an increased incidence of late stent thrombosis, particularly after discontinuation of thienopyridine therapy, as well as of delayed onset of restenosis or catch-up phenomenon with DESs. Based on animal and human pathological data, investigators have linked the above-mentioned concerns to the presence of polymers in DESs, which have a proinflammatory and prothrombinogenic potential, and sometimes may induce a hypersensitivity reaction. This trial will compare the anti-restenotic efficacy of the permanent polymer (PP), biodegradable polymer (BP) and polymer-free (PF) rapamycin-eluting stents in patients with coronary artery disease. Cypher stent (PP) is a stainless steel stent coated with sirolimus with use of permanent polymers while the ISAR stent is a rough surface stainless steel stent which allows not only polymeric coating (for example biodegradable polymer, BP ISAR stent) but also coating without the need of polymer (PF ISAR stent) in the cath lab.

Study Timeline

• Study Start: 2006-06
• Study First Submitted: 2006-07-07
• Study First Submitted QC: 2006-07-07
• Study First Posted: 2006-07-10
• Primary Completion: 2007-09
• Study Completion: 2007-10
• Status Verified: 2008-01
• Last Update Submitted: 2008-01-10
• Last Update Posted: 2008-01-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 605

Inclusion Criteria

• Patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥50% de novo stenosis located in native coronary vessels.
• Written, informed consent by the patient or her/his legally-authorized representative for participation in the study.

Exclusion Criteria

• Target lesion located in the left main trunk or bypass graft.
• In-stent restenosis.
• Cardiogenic shock.
• Malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
• Known allergy to the study medications: aspirin, clopidogrel, rapamycin, stainless steel.
• Pregnancy (present, suspected or planned) or positive pregnancy test.
• Previous enrollment in this trial.
• Patient's inability to fully cooperate with the study protocol.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
B	polymer-free, rapamycin-eluting stent	polymer-free drug eluting stent PF stent
A	rapamycin-eluting stent with biodegradable polymer	Drug eluting stent using biodegradable polymer BP stent
C	rapamycin-eluting Stent with permanent polymer	permanent polymer using stents PP stent

Primary Outcome Measures

Name	Time	Method
in-stent late luminal loss	at 6 to 8-month follow-up angiogram

Secondary Outcome Measures

Name	Time	Method
Need of target lesion revascularization	at 9-month follow-up
Incidence of stent thrombosis.	at 9-month follow-up
In-segment binary angiographic restenosis	at 6 to 8-month follow-up angiogram
Combined incidence of death or myocardial infarction	at 9-month follow-up

Trial Locations

Locations (2)

1. Medizinische Klinik, Klinikum rechts der Isar; 🇩🇪 Muenchen, Germany

Deutsches Herzzentrum Muenchen; 🇩🇪 Munich, Germany