Test of Long-Term Safety and Efficacy of Sirolimus-Permanent-Polymer Eluting Stent (Cypher)- and Sirolimus-Polymer-free Eluting Stents (PPS/PFS) Assessed by Optical Coherence Tomography (PPS/PFS-OCT)

German Heart Center Munich

Status and phase: Unknown; Phase 4

Conditions: Coronary Heart Disease

Treatments: Device: Sirolimus-Polymer-free Eluting Stent; Device: Sirolimus-Permanent-Polymer Eluting Stent

Study type: Interventional

Funder types: Other

Identifiers

NCT01260558

GE IDE No. S03310

Details and patient eligibility

About

The objective of this pilot study is to compare the PFS-eluting stent (ISAR Rapa G1) with the PPS-eluting stent (Cypher®) regarding uncovered stent strut segments at 5 years.

Full description

The mid-term efficacy of drug-eluting stents has been well-established, but 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 permanent polymer-based DES. The extent of strut coverage with reduction of exposed thrombogenic material has been shown to be associated with the inflammatory reaction grade and with the incidence of stent thrombosis. The optical coherence tomography (OCT) is an intravascular imaging modality based on light. The principle is similar to intravascular ultrasound, but due to the much shorter wave length of light, it offers a much better resolution up to 10µm, enabling the exact determination of strut coverage, neointimal thickness, vessel size, presence of dissections, and even the presence of inflammation.

Patients who received a polymer-free or a permanent-polymer sirolimus-eluting stent about 5 years ago without in-segment intervention since, will be evaluated by OCT regarding the healing pattern and the late lumen loss of the stent.

Enrollment: 20 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients older than age 18 with with previous implantation of polymer-free or permanent-polymer sirolimus-eluting stents 5 years ago due to ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% stenosis located in native coronary vessels.
• Written, informed consent by the patient or her/his legally-authorized representative for participation in the study and assessment by OCT.
• In women with childbearing potential a negative pregnancy test is mandatory.

Exclusion criteria

• Intervention in the segment of the study stent after the index procedure
• Target lesion located in the left main trunk.
• In-stent restenosis with difficulty to pass the OCT device
• Acute myocardial infarction
• Known allergy to the study medications: Sirolimus, rapamycin, probucol or stainless steel.
• Pregnancy (present, suspected or planned) or positive pregnancy test.
• Patient's inability to fully cooperate with the study protocol.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

Arm 1

Active Comparator group

Description:

Sirolimus-Permanent-Polymer Eluting Stent

Treatment:

Device: Sirolimus-Permanent-Polymer Eluting Stent

Arm 2

Active Comparator group

Description:

Sirolimus-Polymer-free Eluting Stent

Treatment:

Device: Sirolimus-Polymer-free Eluting Stent