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Stents clinical trials

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NCT ID: NCT05872074 Recruiting - Stents Clinical Trials

Immediate and Short Term Outcomes for Using Drug Coated Balloons in Treating Coronary Bifurcation Lesions

DCB
Start date: October 4, 2023
Phase: N/A
Study type: Interventional

● the investigators aims to study the impact of using drug coated balloon in coronary artery bifurcation lesions on the procedural success rate & short-term MACE.

NCT ID: NCT05556668 Completed - Biliary Stricture Clinical Trials

Percutaneous Biodegradable Biliary Stents for the Treatment of Benign Biliary Strictures.

Start date: August 20, 2022
Phase:
Study type: Observational

To assess safety and effectiveness in the long term of percutaneous insertion of Biodegradable (BD) Biliary Stents for the treatment of benign biliary strictures, in a single center experience.

NCT ID: NCT04115696 Completed - Stenosis Clinical Trials

Biodegradable Stent Implantation in Biliary Benign Strictures.

BiELLA
Start date: March 1, 2012
Phase:
Study type: Observational [Patient Registry]

Spanish registry of resorbable stent implantation in biliary benign strictures. This registry is sponsored by the Spanish Society of Vascular and Interventional Radiology (SERVEI) and conducted by the Research Group GITMI (Group of Research in Minimally Invasive Techniques) of the University of Zaragoza (Spain). A software tool hosted on the official website of SERVEI and the journal Intervencionismo will be used for data collection a(https://estudios.watsoncme.com).

NCT ID: NCT03989557 Completed - Stents Clinical Trials

Application of Platelet Function Test in Prevention of Ischemic Events After Stent Placement in Intracranial Aneurysms

APISIA Trail
Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

This study was designed to identify high platelet reactivity (HPR) who might have in-stent thrombosis in unruptured aneurysm with intracranial stent placement with light transmittance platelet aggregometry (LTA). For HPR patients, higher ischemic stroke rate maybe occurred, and we hypothesis that dose adjustment of aspirin and clopidogrel based on LTA monitoring maybe reduces the rate of ischemic stroke compared to a standard strategy after intracranial stent implantation at early periprocedural period and 1 month follow-up period.

NCT ID: NCT03521700 Completed - Blood Pressure Clinical Trials

Compare Effects of Intensive Versus Conventional Lipid-lowering Therapy in Patients With Severe Atherosclerotic Renal Artery Stenosis Undergoing Stent Placement

Start date: June 1, 2013
Phase: Phase 2/Phase 3
Study type: Interventional

Although expert consensuses recommend the use of statins in the treatment of atherosclerotic renal artery stenosis, in patients with severe atherosclerotic renal artery stenosis undergoing stent placement, the related investigation focused on renal protection by intensive lipid-lowering therapy is scant , and the optimal target level for lipid reduction remain uncertain. Therefore, we hypothesized that intensive lipid lowering could offer more benefits with respect to renal function in the patients with percutaneous renal artery stenting. We conducted the prospective randomized unblinded trial to compare the renal-protective effect of intensive lipid lowering with that of conventional lipid lowering in patients underwent renal artery stenting (75 patients in each study group)

NCT ID: NCT03375411 Withdrawn - Clinical trials for Coronary Artery Disease

First-in-Man Study: Safety and Efficacy of INC-1 Bare Metal Stent in the Novo Coronary Lesions.

Start date: December 30, 2017
Phase: N/A
Study type: Interventional

This is a First In Man study with the aim to know the safety and effectiveness of a novel bare metal stent (INC-1) in the treatment of de novo coronary lesions in patients with stable coronary angina and unique coronary lessions.

NCT ID: NCT03119012 Terminated - Clinical trials for Coronary Artery Disease

P2Y12 Inhibitor Monotherapy Versus Extended DAPT in Patients Treated With Bioresorbable Scaffold

SMART-CHOICEII
Start date: April 19, 2017
Phase: Phase 4
Study type: Interventional

This study aimed to compare the efficacy and safety of P2Y12 inhibitor monotherapy versus extended dual antiplatelet therapy (DAPT) following 12-month of DAPT in patients undergoing percutaneous coronary intervention (PCI) with bioresorbable scaffold (BRS)

NCT ID: NCT02811796 Completed - Prognosis Clinical Trials

Angio-based Fractional Flow Reserve to Predict Adverse Events After Stent Implantation

HAWKEYE
Start date: June 2016
Phase:
Study type: Observational

The investigators will collect prospectively baseline, procedural and follow-up data of all patients receiving successful percutaneous coronary intervention (PCI) and stent implantation. Angio-based flow fractional reserve (quantitative flow ratio, QFR, Medis medical imaging systems Leiden, The Netherlands) will be estimated in all patients. Especially, the investigators at the end of the procedure (this is defined according operator's judgement) will record 2 orthogonal angiograms (as suggested by QFR instructions) at 15 frames/second and the same 2 orthogonal angiograms at 30 frames/second. An independent corelab (blinded to procedural data and clinical outcome) will estimate QFR value (one with the angiograms at 15 frames and one with those at 30 frames

NCT ID: NCT01997242 Recruiting - SURGERY Clinical Trials

The Surgery After Stenting (SAS) Registry

SAS registry
Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

The SAS registry will include any patient with previous coronary stenting undergoing any type of surgery or operative endoscopic/endovascular procedure at the participating Centers. The relevant clinical, procedural and outcome data (within index surgical admission and at 30 days) will be entered in a specifically designed electronic case record form (eCRF).

NCT ID: NCT01962168 Completed - Neoplasms Clinical Trials

Evolution® Biliary Stent System Clinical Study

Start date: December 2013
Phase: N/A
Study type: Observational

The Evolution® Biliary Stent System Clinical Study is a clinical trial on a commercially available device to gather physician experience with the Cook Evolution® Biliary Stent System for the palliation of cancer in the biliary tree. Patients will be treated as per usual medical practices.