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Safety and Efficacy Registry of Yinyi Stent (SERY-II)

Safety and Efficacy Registry of Yinyi Polymer-free Paclitaxel-eluting Stent

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01373658
Acronym
SERY-II
Enrollment
200
Registered
2011-06-15
Start date
2010-05-31
Completion date
2011-12-31
Last updated
2011-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Brief summary

Drug-eluting stents effectively reduce restenosis but may increase late thrombosis and delayed restenosis. Persistent polymer could be responsible. Local delivery of paclitxel from a polymer-free Yinyi stent (Dalian Yinyi biomaterial research and development co.ltd) may prevent these complications.

Interventions

subjects with Yinyi stent implantation

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* age 18-80 years old * both gender * native coronary lesion * narrowing \> 70% * vessel size 2.5-4.0 in diameter

Exclusion criteria

* without informed consent, * ST elevation myocardial infarction within 7 days, * patient with ≤ 70% coronary narrowing at target lesion, * left main lesion, * multivessel narrowing need more than 3 stent implantations, * by-pass graft, * abnormal liver function before randomization, * active hepatitis or muscular disease, * impaired renal function with serum creatinine level \> 3mg/dl, * impaired left ventricular function with LVEF \< 30%, * participate in other studies.

Design outcomes

Primary

MeasureTime frameDescription
late lumen loss12 monthsLate luminal loss was defined as the difference between the minimal luminal diameter immediately after the placement of the stent and the minimal luminal diameter at 12-month angiographic follow-up.

Secondary

MeasureTime frameDescription
major adverse cardiac events12 monthsincluding cardiac death, re-infarction, and target vessel revascularization

Countries

China

Contacts

Primary ContactRuiyan Zhang, MD
zhangruiyan@263.net862164370045

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026