Clinical Trials Logo

Clinical Trial Summary

Percutaneous treatment of bifurcation lesion is a complex procedure. After main vessel stent implantation, the side branch became jailed and the carina can be displaced resulting in complete occlusion of this vessel. Re-wiring the side branch in this conditions may result difficult and some times impossible. There is no agreement regarding the need of side branch pre-dilation (before main vessel stent implantation) to reduce these complications. Researchers from European Bifurcation Club have proposed no to pre-dilate the side branch to avoid vessel dissection and difficulties in rewiring the true lumen of the vessel. On the contrary, our group has a good experience in the treatment of bifurcation lesions treated with side branch pre-dilation.

Aims: 1.- To determine the efficacy of the side-branch pre-dilation in patients with bifurcations lesions treated with provisional T stenting. 2.- To determine the success rate and incidence of complications in patients with and without side-branch pre-dilation, as well as economic impact in terms of number of used wires.


Clinical Trial Description

Introduction: Percutaneous treatment of bifurcation lesion is a complex procedure. After main vessel stent implantation, the side branch became jailed and the carina can be displaced resulting in complete occlusion of this vessel. Re-wiring the side branch in this conditions may result difficult and some times impossible. There is no agreement regarding the need of side branch pre-dilation (before main vessel stent implantation) to reduce these complications. Researchers from European Bifurcation Club have proposed no to pre-dilate the side branch to avoid vessel dissection and difficulties in rewiring the true lumen of the vessel. On the contrary, our group has a good experience in the treatment of bifurcation lesions treated with side branch pre-dilation.

Aims: 1.- To determine the efficacy of the side-branch pre-dilation in patients with bifurcations lesions treated with provisional T stenting. 2.- To determine the success rate and incidence of complications in patients with and without side-branch pre-dilation, as well as economic impact in terms of number of used wires.

Design: Prospective and randomized study. Patients and methods: The series is constituted by 420 patients with bifurcations lesions that will be treated with drug-eluting stents; 210 patients will be treated with side branch pre-dilation before main vessels stent implantation, while the remaining 210 patients will be randomized to no pre-dilation of the side-branch.

Primary end point:

- TIMI flow at Side Branch after main vessel stent implantation.

Secondary end points:

- Time of re-wiring.

- Number of used wires.

- % of stenosis at Side Branch.

- Levels of CK and TpI after the procedure.

- Related cardiac events at 9 months. Relevance: Currently there has been controversy over the use of the side branch pre-dilation in patients with bifurcations lesions treated with provisional T-stenting. However, we have no comparative study in the literature. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01090856
Study type Interventional
Source Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
Contact
Status Completed
Phase Phase 4
Start date February 2009
Completion date May 2013

See also
  Status Clinical Trial Phase
Completed NCT01239225 - Prevalence of Abdominal Aortic Aneurysm in Patients Undergoing Coronary Angiography Phase 4
Recruiting NCT05075590 - Coronary Access After Supra-Annular THV Implantation N/A
Completed NCT02606734 - DyeVert Pilot Trial N/A
Completed NCT00632918 - Effects of Heart Rates and Variability of Heart Rates on Image Quality of Dual-Source CT Coronary Angiography N/A
Completed NCT04801901 - Distal Transradial Access for Percutaneous Coronary Intervention N/A
Completed NCT00345501 - Iloprost for Prevention of Contrast-Mediated Nephropathy in High-Risk Patients Undergoing Coronary Angiography and/or Intervention Phase 2/Phase 3
Recruiting NCT04521660 - The Effect of Using Virtual Reality Glasses During Coronary Angiography N/A
Completed NCT05982366 - Feasibility and Safety of the Routine Distal Transradial Approach N/A
Recruiting NCT04982419 - Remote Ischemic Preconditioning for Renal and Cardiac Protection in Congestive Heart Failure (RICH) Trial Phase 2/Phase 3
Completed NCT00468195 - Optimizing Image Quality in Obese Patients Undergoing Coronary Computed Tomography (CT) Angiography N/A
Completed NCT00468325 - Coronary Computed Tomography for Systematic Triage of Acute Chest Pain Patients to Treatment (CT-STAT) N/A
Completed NCT04911218 - GlideSheath Slender® Versus Conventional 5Fr Arterial Sheath in Coronary Angiography Through the Distal Radial Artery N/A
Completed NCT04318990 - DIstal vs Proximal Radial Artery Access for Cath N/A
Recruiting NCT06312397 - The Effect on Back Pain and Fatigue Level of Acupressure N/A
Recruiting NCT05319119 - Fractional Flow Reserve Derived From CT Related Treatment
Not yet recruiting NCT05133206 - Fasting or Non-fasting Before Cardiac Catheterization N/A
Completed NCT02818101 - Hypnosis Efficacy for the Prevention of Anxiety During a Coronary Angiography N/A
Completed NCT00465335 - Usefulness of Coronary CT Angiography in Patients With Inconclusive Stress Test Results N/A
Recruiting NCT06035783 - Calcium Reduction by Orbital Atherectomy in Western Europe
Completed NCT04407936 - Risk Factors and Prognosis of Adverse Cardiovascular and Kidney Events After Coronary Intervention