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SORT-OUT V - Randomised Clinical Comparative Study of the Nobori and the Cypher Stent.

Phase 4
Completed
Conditions
Coronary Artery Disease
Angina Pectoris
Interventions
Procedure: Percutaneous coronary intervention (PCI)
Registration Number
NCT01254981
Lead Sponsor
Aarhus University Hospital Skejby
Brief Summary

To perform a randomized comparison between the Cypher Select+ stent and the Nobori stent in the treatment of unselected patients with ischaemic heart disease.

Detailed Description

All patients to be treated with one or several drug-eluting coronary stents at one of the four heart centers in Odense, Skejby, Aalborg and Varde can be included in the study. All patients enrolled in the study will be hospitalized at one of the heart centers mentioned. Patients will not be recruited via advertisements.

The study is designed as a non-inferiority study, where the objective is to prove that Nobori is Δ0 poorer as a maximum than Cypher select+. The nine-month event rate (cardiac death, MI and/or TVR) in the Cypher stent group of SORT OUT 3 was 3.0%

The calculation of power below has been made under the following assumptions:

P (Cypher) = 0.03

There is no good estimate for the event rate related to the Nobori stent. α = 0.05 - one-sided

1-β = 0.80

Based on the various values of Δ0 the necessary number of patients, N, in each group can be calculated (StudySize Version 2.0.4, Creostat):

* Δ0 \*N in each group

* 0.0025 \*57,589

* 0.005 \*14,397

* 0.010 \*3,599

* 0.015 \*1,599

* 0.020 \*900

According to the above assumptions, a total of 900 patients must be included in each group in order to reject a null hypothesis that the event rate in the Nobori group is more than 2 percentage points (0.02) poorer than the event rate in the Cypher group or that Nobori is inferior to Cypher, (H0: pNobori - pCypher ≥ Δ0 = 0.02). The alternative hypothesis (HA: pN - pS \< Δ0) provides that Nobori is non-inferior to Cypher - with the selected limit for non-inferiority.

Assuming an inclusion rate of 200 patients per month, it will be possible to include 2000 patients in 10 months.

Power is almost 0.9 if the inclusion is increased to a little over 2400.

Organization

The study is headed by a steering committee, in which PCI operators will participate from each of the participating sites.

Evald Høj Christiansen, Aarhus, will be Principal Investigator. At present, the other members of the steering committee are: Jens Flensted Lassen (chairman), Leif Thuesen, Jan Ravkilde, Hans-Henrik Tilsted, Per Thayssen and Lisette Okkels Jensen. All members of the steering committee will be given full access to the database and will take part in the interpretation of data.

The study secretariat and the randomization computer are localized at the Department of Cardiology, \[Hjertemedicinsk Afdeling\], Aarhus University Hospital, Skejby.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
2504
Inclusion Criteria

All patients eligible for treatment with one or several drug-eluting coronary stents at one of the four heart centers in Odense, Skejby, Aalborg or Varde can be included in the study.

The patients will be treated in accordance with the criteria applicable at the individual sites. The indication for using DES varies slightly between the four sites, as the indication for implantation of DES is based on clinical and angiographic criteria with the financial constraints applying at the individual site. Basically, DES will be chosen instead of BMS in patients with an estimated increased risk of restenosis, in patients with the following stenosis types: Long lesions, lesions in small vessels, bifurcations, ostial lesions, in-stent restenoses and stenosis in the proximal segment of the anterior descending branch. Furthermore, DES will also be chosen for diabetics and in the left main.

Exclusion Criteria
  • The patient does not wish to participate
  • The patient is participating in other randomized stent studies
  • Life expectancy < 1 year
  • Allergic to Aspirin, clopidogrel, prasugrel or ticlopidin
  • Allergic to sirolimus or biolimus

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
NoboriPercutaneous coronary intervention (PCI)Percutaneous coronary intervention with implantation of coronary stent (Nobori)
CypherPercutaneous coronary intervention (PCI)Percutaneous coronary intervention with implantation of coronary stent (Cypher)
Primary Outcome Measures
NameTimeMethod
Primary outcomeWithin 9 months

Major Adverse Cardiac Events, such as cardiac death, myocardial infarction, stent thrombosis or target lesion revascularisation: repeated revascularisation of an index lesion at PCI or bypass surgery

Secondary Outcome Measures
NameTimeMethod
Major Adverse Coronary Events30 days

Cardiac death, myocardial infarction, target vessel revascularisation: repeated revascularisation of an index lesion at PCI or bypass surgery

Acute Myocardial Infarction30 days and 9 months
Target lesion revascularisation defined as repeated revascularisation of an index lesion at PCI or bypass surgery.9 and 12 months and 3 years
Death30 days and 9 months
Secondary outcome

* Device success rate defined as the frequency of a successful implantation of the study stent in all the stenoses scheduled to be treated with residual stenosis \< 20

* Procedural success rate defined as the frequency of successful implantation of the study stent in all the stenoses scheduled to be treated with residual stenosis \< 20% and without serious complications (MACE = Major Adverse Coronary Events))

* Procedural time defined as time from guiding catheter in to guiding catheter out

* X-ray time

* Use of contrast medium

Stent thrombosis12, 24 and 36 months

Defined in accordance with the ARC definition of stent thrombosis

Trial Locations

Locations (3)

Odense University Hospital

🇩🇰

Odense, Denmark

Aarhus University Hospital, Skejby

🇩🇰

Aarhus N, Denmark

Aalborg Universitetshospital

🇩🇰

Aalborg, Denmark

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