The Study of the Crushing Technique Application Using SES in Coronary Bifurcations.

Coronary Artery Disease Clinical Trial

— CACTUS  

Official title:

CORONARY BIFURCATIONS: APPLICATION OF THE CRUSHING TECHNIQUE USING SIROLIMUS-ELUTING STENTS - The "CACTUS" Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00749424
• Other study ID #: CRDIT 00-01/03
• Status: Completed
• Phase: Phase 4
• First received: September 8, 2008
• Last updated: February 3, 2010
• Start date: January 2004
• Est. completion date: April 2009

Study information

• Verified date: February 2010
• Source: Cordis Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to compare the safety and effectiveness of two different approaches to treat bifurcational lesions with CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent , Cordis Corp): a) the "crushing" technique to stent both branches vs. b) a provisional T stenting technique of the side branch.

Description:

This is a prospective, randomized study that will be conducted at up to 5 centers in Italy. All patients who meet the eligibility criteria will be treated with the Cypher SelectTM Stent and Stent Delivery System (SDS). Patients will have repeat angiography at six months, with clinical follow-up to 2 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 350
• Est. completion date: April 2009
• Est. primary completion date: May 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Is a male or non-pregnant female patient >= 18 years of age [NOTE: Females of child-bearing potential must have a negative pregnancy test];

2. Has a diagnosis of angina pectoris as defined by Canadian Cardiovascular Society Classification (CCS I, II, III, IV) OR unstable angina pectoris (Braunwald Classification B&C, I-II) OR has documented silent ischemia;

3. Has at least TIMI I coronary flow in both the main and side branches;

4. Involves a single treatment of a de novo bifurcation lesion in native coronary arteries of patients with single or multivessel disease; patients with multiple lesions can be included only if other lesions treated during the index procedure are successfully treated prior to the treatment of the bifurcation lesion;

5. Has a true bifurcation lesion defined as stenosis > 50% in both the main branch and the ostium of the side branch;

6. Has a maximum treatable main or side branch lesion length <=28 mm;

7. Has a main branch vessel that is >= 2.5 mm and <= 3.5 mm in diameter by on-line QCA proximal to the bifurcation;

8. Has a side branch vessel that is >= 2.25 mm and <= 3.5 mm in diameter by on-line QCA;

9. Is an acceptable candidate for coronary artery bypass surgery (CABG);

10. Is willing to comply with the specified follow-up evaluation;

11. The patient or legally authorized representative must provide written informed consent prior to the procedure.

Exclusion Criteria:

1. Patient has experienced a Q-wave or non-Q-wave myocardial infarction with documented elevation of CK levels > 2 times normal or CK-MB levels > 3 times normal within the preceding 24 hours and/or the CK and CK-MB enzymes remain above normal at the time of treatment;

2. Has unstable angina classified as Braunwald A I-III, B&C III;

3. Has a bifurcation lesion in a non protected left main;

4. Has an ejection fraction <= 35%;

5. Has known allergies to the following: aspirin, clopidogrel bisulfate (Plavix) and ticlopidine (Ticlid), heparin, or sirolimus;

6. Has a known serious allergy to contrast media or stainless steel that cannot be managed medically;

7. Has impaired renal function (creatinine > 3.0 mg/dl);

8. There is presence of thrombus in the bifurcation lesion;

9. Has a target lesion with excessive tortuousity unsuitable for stent delivery and deployment;

10. Has a totally occluded vessel;

11. Is the recipient of a heart transplant;

12. Has a significant medical condition which in the investigator's opinion may interfere with the patient's optimal participation in the study;

13. Is currently participating in an investigational drug or another device study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Disease
• Myocardial Ischemia

Intervention

Device:
• SES
CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent
• SES
CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent

Locations

Country	Name	City	State
Italy	Fondazione Centro San Raffaele del Monte Tabor	Milano

Sponsors (1)

Lead Sponsor	Collaborator
Cordis Corporation

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Colombo A, Bramucci E, Saccà S, Violini R, Lettieri C, Zanini R, Sheiban I, Paloscia L, Grube E, Schofer J, Bolognese L, Orlandi M, Niccoli G, Latib A, Airoldi F. Randomized study of the crush technique versus provisional side-branch stenting in true coro — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Major Adverse and Cardiac Events (MACE)		6 and 12 months post-procedure	Yes
Secondary	Minimal lumen diameter (MLD)		6 months	Yes
Secondary	Percent diameter stenosis (%DS)		6 months	Yes