Overview

This trial is active, not recruiting.

Condition coronary artery diseases
Treatment stent
Sponsor Medfavour (Beijing) Medical Co., Ltd
Collaborator Fuwai Hospital,National Center for Cardiovascular Diseases,China
Start date April 2009
End date December 2010
Trial size 300 participants
Trial identifier NCT01226355, FW2009-183

Summary

A single blind, multi-center, randomized study is preformed to compare NOYA CoCr biodegradable coating sirolimus-eluting stents with Firebird2 drug-eluting stents from MicroPort Medical (Shanghai) Co., Ltd. to evaluate the safety and efficacy of NOYA CoCr biodegradable coating sirolimus-eluting stents in treating coronary artery lesions.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking single blind (outcomes assessor)
Primary purpose treatment
Arm
(Experimental)
implant NOYA CoCr Biodegradable Coating Sirolimus-Eluting Stents Intervention: Device: stent
stent NOYA CoCr Biodegradable Coating Sirolimus-Eluting Stent System
NOYA CoCr Biodegradable Coating Sirolimus-Eluting Stent System is manufactured by Medfavour (Beijing) Medical Co., Ltd. Firebird drug-eluting stents from MicroPort Medical (Shanghai) Co., Ltd.
(Active Comparator)
implant Firebird2 drug-eluting stents Intervention: Device: stent
stent NOYA CoCr Biodegradable Coating Sirolimus-Eluting Stent System
NOYA CoCr Biodegradable Coating Sirolimus-Eluting Stent System is manufactured by Medfavour (Beijing) Medical Co., Ltd. Firebird drug-eluting stents from MicroPort Medical (Shanghai) Co., Ltd.

Primary Outcomes

Measure
In-stent late loss at 9-month
time frame: 270 days (±30days)

Secondary Outcomes

Measure
MACEs found in follow-up period
time frame: 5 years

Eligibility Criteria

Male or female participants from 18 years up to 75 years old.

Inclusion Criteria: 1. Age 18-75 years, men or unpregnant women; 2. Angina pectoris patients with non-symptom myocardial ischemia, or patients with obsolete myocardial infarction; 3. Total of lesion artery ≤2; 4. Lesion artery ≤30 mm in length, 2.25 to 4.0 mm in diameter (ocular estimate); 5. Narrow level of lesion artery ≥70% in diameter (ocular estimate); 6. Amount of same stents implanted in a lesion artery ≤2; 7. Patients with indications of coronary artery bridging surgery(coronary artery bypass transplant technique); 8. Patients knowing about the objective of trial, willing to sign a statement of informed consent and join in this trial, and willing to accept follow-up. Exclusion Criteria: 1. Patients with acute myocardial infarction in 7 days; 2. Chronic total occlusion lesions(TIMI 0 grade blood flow prior to implantation), left trunk vessel lesion, three-branch lesions needing treated, fork and bridge vessel lesions of branch vessels whose diameter ≥2.25mm; 3. Severe calcific lesions and twisted lesions which cannot be pre-expanded, and lesions unsuitable for delivering and expanding stents; 4. In-stent restenosis lesions; 5. Patients with stent implantation in his/her coronary artery within recent one year; 6. Severs heart failure(over NYHA III grade ), or left ventricular ejection fraction(LVEF)< 40%( supersonic inspection or left ventricular radiography ); 7. Kidney functional damage prior to implantation, serum creatinine level>2.0mg/dl; 8. Patients with hemorrhage tendency, an active digestive ulcer history, a cerebral hemorrhage or subarachnoid hemorrhage history, or cerebral apoplexy within half a year, and these patients who contraindicate against platelet inhibitors and anticoagulant therefore can not bear anticoagulation treatment; 9. Patients allergic to aspirin, clopidogrel or ticlopidine, heparin, contrast medium, rapamycin and metals; 10. Patients whose life expectancy less than 12 months; 11. Patients who are participating in other drugs or medical devices clinical trials; 12. Patients who can not comply with the clinical trial protocol; 13. Patients having a heart transplant.

Additional Information

Official title Clinical Trial Program of a Medical Instrument Product
Principal investigator Runlin Gao, Professor
Description A single blind, multi-center, randomized study is preformed to compare NOYA CoCr biodegradable coating sirolimus-eluting stents with Firebird2 drug-eluting stents from MicroPort Medical (Shanghai) Co., Ltd. to evaluate the safety and efficacy of NOYA CoCr biodegradable coating sirolimus-eluting stents in treating coronary artery lesions. Appropriate patients judged by inclusion and exclusion standards will be preformed stent implantation, and after that all patients will be clinically followed up at 30, 90, 180, 270,365 days,2 years,3 years,4 years and 5 years. Especially, standard quantity coronary angiography (QCA) will be conducted at 270 days (±30days) through which the main therapeutic indicator of late luminal loss (LLL) is obtained so as to evaluate the efficacy of tested stents. Major adverse cardiac events (MACEs) found in following-up period as key indicators to evaluate the safety of stents. The arrangement, conclusion and statistical analysis of trial data including clinography and angiography will be fulfilled by independent Data Management Center(DMC) and radiography core laboratory.
Trial information was received from ClinicalTrials.gov and was last updated in May 2012.
Information provided to ClinicalTrials.gov by Medfavour (Beijing) Medical Co., Ltd.