Clinical Trial on the Efficacy and Safety of Sirolimus-Eluting Stent (MiStent® System)

Coronary Heart Disease Clinical Trial

— DESSOLVE-C  

Official title:

A Prospective, Single-blinded, Multi-center, Randomized, Controlled, Registered Clinical Trial on the Efficacy and Safety of Sirolimus-eluting Stent (MiStent® System) in the Treatment of Patients With Coronary Heart Disease

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02448524
• Other study ID #: MiStent01
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: July 2015
• Est. completion date: November 2022

Study information

• Verified date: September 2020
• Source: Micell Technologies
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

• To evaluate the safety and efficacy of MiStent drug (sirolimus)-eluting stent system in the treatment of coronary heart disease (CHD) in patients with primary in situ CHD (de novo);

• To evaluate operating performance of the MiStent drug (sirolimus)-eluting coronary stent system.

Description:

• The study will enroll a total of 428 cases of primary in situ coronary artery disease patients (all patients enrolled with a maximum of two target lesions in different blood vessels and maximum of 2 stents per lesion. If more stents are needed for implantation, stents with the same brand are required, and mixing brands is not allowed for each patient except for salvage with implantation of other brand of stents.)

• Lesions with reference diameter of 2.5mm-3.5mm (by visual measurement) and with length ≤40mm (by visual measurement) will be selected, subjects meeting the inclusion and exclusion criteria and who agree to participate will be enrolled.

• Prospective, single-blinded, multi-center, randomized, controlled clinical trial;

• Patients with in situ primary CHD;

• Clinical sites: up to 18; patients will be enrolled in a 1:1 ratio (i.e., 214 cases enrolled into each group, the MiStent stent group and TIVOLI stent group);

• Clinical follow-up time points: 1 month, 6 months, 9 months, 12 months and yearly at 2-5 years post index procedure;

• Angiographic follow-up at 9 months post index procedure; in-stent late lumen loss measured by quantitative coronary angiography (QCA) will be used as the primary efficacy endpoint for product evaluation;

• In this trial, the collection, collation, statistical analysis and adjudication of all relevant clinical and angiographic data will be conducted by an independent coronary angiography core laboratory (CCRF Medical Technology Co., Ltd.), data management and statistical center, clinical events committee and clinical audit agency. All patients will be followed up for 5 years (by telephone or outpatient form), and the incidence of adverse events will be recorded to allow a more accurate and reliable evaluation of the long-term safety of the MiStentTM drug (sirolimus) eluting coronary stent system.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 428
• Est. completion date: November 2022
• Est. primary completion date: November 30, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Stable and unstable angina pectoris (AP), old myocardial infarction (OMI), or confirmed evidence of myocardial ischemia;

• Primary in situ coronary artery lesions (up to two target lesions and up to 2 stents per lesion);

• Visual target lesion length =40mm;

• Visual reference vessel diameter of 2.5-3.5mm;

• Visual diameter stenosis =70%;

• Patients with indications for coronary artery bypass surgery (CABG);

• Subjects participate voluntarily and signed an informed consent willing to accept angiographic and clinical follow-up.

Exclusion Criteria:

• Acute myocardial infarction (AMI) occurred within 7 days prior to the procedure; post-MI complicated with elevated levels of cardiac enzymes (CK-MB, cTNT / I);

• CTO (TIMI-0) lesions, left main lesions, ostial lesions,bypass graft lesions, bifurcation lesions (lateral side branch reference vessel diameter=2.5mm), restenosis in-stent and three-vessel disease that need to be treated;

• Severe calcified lesions for which balloon pre-dilation is expected to be unsuccessful;

• Tortuous lesions that render stent crossing difficult;

• NYHA class=III or left ventricular ejection fraction <40%;

• Implantation of other stents in the past year;

• Pregnant or breast-feeding patients or patients planning to get pregnant within the following year;

• Subjects with bleeding tendency or coagulation disorder or PCI contraindications and / or anticoagulant therapy contraindications or who have not tolerated dual antiplatelet treatment within a year to date;

• Presence of other diseases (such as cancer, malignancies, congestive heart failure, organ transplantation or candidate for it) or history of substance abuse (alcohol, cocaine, heroin, etc.), poor protocol compliance or life expectancy of less than 1 year;

• Allergic to one of following: aspirin, heparin, clopidogrel, sirolimus (rapamycin), PLGA polymers, contrast agents and metal;

• Severe liver and kidney dysfunction (ALT or AST level 3 times greater than the upper limit of normal; eGFR <30ml/min);

• Patients participating in any other clinical trial and who have not completed follow-up to the primary endpoint;

• Study subjects with poor compliance judged by investigators, with poor possibility to complete study in accordance with requirements.

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Disease
• Coronary Heart Disease
• Heart Diseases
• Myocardial Ischemia

Intervention

Device:
• MiStent
Primary in situ coronary artery disease patients (all patients enrolled with a maximum of two target lesions in different blood vessels and maximum of 2 stents per lesion. Lesions with reference diameter of 2.5mm-3.5mm (by visual measurement) and with length =40mm (by visual measurement).
• TIVOLI
Primary in situ coronary artery disease patients (all patients enrolled with a maximum of two target lesions in different blood vessels and maximum of 2 stents per lesion. Lesions with reference diameter of 2.5mm-3.5mm (by visual measurement) and with length =40mm (by visual measurement).

Locations

Country	Name	City	State
China	The General Hospital of Shenyang Military Region	Area Of Shenyang
China	The First Affiliated Hospital of Baotou University	Baotou	Inner Mongolia
China	Fu Wai Hospital, National Center for Cardiovascular Disease	Beijing
China	The First Hospital of Jilin University	Changchun
China	The Second Xiangya Hospital of Central South University	Changsha
China	The Third Xiangya Hospital of Central South University	Changsha	Hunan
China	Sir Run Run Shaw Hospital School of Medicine, Zhejiang University	Hangzhou	Zhejiang
China	Inner Mongolia People'S Hospital	Hohhot	Inner Mongolia
China	The First Affiliated Hospital of Inner Mongolia Medical University	Hohhot	Inner Mongolia
China	The First Hospital of Lanzhou University	Lanzhou
China	The Second Affiliated Hospital of Nanchang University	Nanchang	Jiangxi
China	Shanghai Ninth People's Hospital	Shanghai
China	West China Hospital, Sichuan University	Sichuan
China	The Second Hospital of Shanxi Medical University	Taiyuan
China	TEDA International Cardiovascular Hospital	Tianjin
China	The First Affiliated Hospital of Xi'An Jiaotong University	Xi'an	Shaanxi

Sponsors (4)

Lead Sponsor	Collaborator
Micell Technologies	CCRF Consulting Co., Ltd., Giant Med-Pharma Services Inc., Hefei Life Science Medical Instruments Co. Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	In-stent late lumen loss (LLL)	Late lumen loss is the difference in millimeters between the diameter of a stented segment post-procedure compared with the follow-up angiogram at nine months	9 months post index procedure
Secondary	Success rate of stent implantation (including device success, lesion success and clinical success);		Baseline
Secondary	Restenosis rate in-stent, at proximal and distal edges of the stent and in-lesion segments; and late lumen loss and percent diameter stenosis in lesion segments		9 months
Secondary	Device-related clinical cardiovascular composite endpoints post index procedure, including cardiac death, target vessel myocardial infarction and clinical symptoms driven target lesion revascularization (i.e., target lesion failure [TLF])		30 days, 6 months, 12 months, and 2-5 years
Secondary	Patient-related clinical cardiovascular composite endpoints post index procedure, including all-cause death (cardiac and non-cardiac), nonfatal myocardial infarction and any revascularization		30 days, 6 months, 12 months and 2-5 years
Secondary	Incidence of ARC-defined stent thrombosis (definite, probable, possible stent thrombosis at early, late and very late periods)		30 days, 6 months, 12 months and 2-5 years
Secondary	Drug-related adverse events of dual antiplatelet therapy (DAPT) post index procedure.		30 days, 6 months, 12 months and 2-5 years