Skip to content

Study of Bifurcation Coronary Stenting in India

A Prospective, Multi-center, Observational Study of Bifurcation Coronary Stenting in India to Determine Clinical and Angiographic Outcomes -Indian Bifurcation Stenting (IBIS) Registry - Indian Bifurcation Stenting (IBIS) Registry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/08/027411
Enrollment
1000
Registered
2020-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: I249- Acute ischemic heart disease, unspecified

Interventions

None listed

Sponsors

Cardiovascular Research Society Kerala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age more than 18 years 2. Any bifurcation coronary stenosis undergoing bifurcation coronary stenting. 3. Two or bifurcations in same patients are eligible, as long as only one bifurcation per vessel. 4. Patients with another single lesion in different vessels could be treated as indicated

Exclusion criteria

Exclusion criteria: 1. Patients with expected survival less than one year 2. Recent CVA 3. Allergic to aspirin, clopidogrel, ticagrelor are excluded 4. Active cancer 5. Inability to provide consent

Design outcomes

Primary

MeasureTime frame
Composite end point of major adverse cardiac events (MACE) includes cardiac death, target lesion myocardial infarction (MI), and ischemia-driven target lesion revascularisation (TLR)Timepoint: 2 years

Secondary

MeasureTime frame
Cardiac death, All-cause mortality, Any Myocardial Infarction (MI), Target lesion myocardial infarction, Target lesion revascularisation (TLR), Stent thrombosis, Target vessel revascularisation, Any Revascularisation and Angina. Number of stents implanted in BCI, Total stent length in BCI, Drug eluting balloon(DEB), Bifurcation strategy, side branch rewiring (SBR) rewiring, Final Kissing Balloon (FKB), Proximal optimisation-side branch-proximal optimisation(PSP) and Imaging.Timepoint: at In-hospital, 1, 12, 24 and 36 months

Countries

India

Contacts

Public ContactDr Rony Mathew

Lisie Hospital

drronymathew@yahoo.com9846097812

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026