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Thailand Orsiro Registry: Safety and Performance Registry for an all-comers patient population with the Limus Eluting Orsiro Stent System within daily clinical practice

Thailand Orsiro Registry: Safety and Performance Registry for an all-comers patient population with the Limus Eluting Orsiro Stent System within daily clinical practice

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20190325001
Enrollment
150
Registered
2019-03-25
Start date
2018-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Subjects requiring coronary revascularization with Drug Eluting Stents (DES) coronary revascularization Drug Eluting Stents (DES) The Limus Eluting Orsiro Stent

Interventions

All&#45
comers patient population with the Limus Eluting Orsiro Stent System.
Supportive Care
The patient with the Limus Eluting Orsiro Stent System

Sponsors

faculty of medicine, chiangmai university
Lead Sponsor
faculty of medicine&#44
Collaborator
chiangmai university
Collaborator

Eligibility

Sex/Gender
All
Age
21 Years to No maximum

Inclusion criteria

Inclusion criteria: - Symptomatic coronary artery disease - Subject signed informed consent for data release - Subject is willing to participate at all follow up assessments - Subject is ≥ 21 years of age

Exclusion criteria

Exclusion criteria: - Subject did not sign informed consent for data release - Known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation / antiplatelet therapy required for PCI, stainless steel, Sirolimus or contrast media - Planned surgery within 6 months of PCI unless dual antiplatelet therapy will be maintained - Pregnancy - Currently participating in another study and primary endpoint is not reached yet.

Design outcomes

Primary

MeasureTime frame
Target Lesion Failure (TLF) at 12 months 12 months Event of cardiac death, Myocardial Infarction (MI), Coronary Artery Bypass Graft (CABG), clinically

Secondary

MeasureTime frame
TLF at 6 months follow up 6 months Clinically driven Target Lesion Revascularization (TLR),Target Vessel Revascularization (TVR) 6 months and 12 months event of Vessel Revascularization ,Target Lesion Revascularization (TLR) at 6 and 12 months Event of lesion revascularization,Stent Thrombosis at 6 and 12 months event Stent Thrombosis ,Clinical Device Success Day 0 number of Clinical Device Success,Clinical Procedural Success Day 0 number of Clinical Procedural Success

Countries

Thailand

Contacts

Public ContactPannipa Suwannasom

Faculty of Medicine, Chiang Mai University

antiann100@gmail.com+66 5393 5486

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026