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Coronary Angioplasty clinical trials

View clinical trials related to Coronary Angioplasty.

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NCT ID: NCT04318990 Completed - Clinical trials for Coronary Angiography

DIstal vs Proximal Radial Artery Access for Cath

DIPRA
Start date: March 6, 2020
Phase: N/A
Study type: Interventional

This single-center, prospective, randomized study will evaluate distal radial artery (dRA) vs. proximal radial artery access (pRA) in regards to hand function and radial artery occlusion.

NCT ID: NCT03817775 Completed - Clinical trials for Coronary Angioplasty

Effect of Music on the Sedative Use During Coronary Angioplasty

Start date: January 31, 2019
Phase: N/A
Study type: Interventional

This is a non-blinded, non-randomized controlled pilot study with no follow-up. Patients will be recruited from the coronary angiography patient pool of the American Hospital of Paris and assigned to one of 2 groups in a non-randomized manner.

NCT ID: NCT03329261 Completed - Clinical trials for Diabetes Mellitus, Type 2

Incidence of Major Cardiovascular Events in Diabetic Patients With ACS Undergoing Coronary Angioplasty and Treated With Clopidogrel 150 mg Versus 75 mg

IDASCOP 1
Start date: December 7, 2017
Phase: Phase 4
Study type: Interventional

Acute Coronary Syndrome (ACS) is triggered by the rupture of an atherosclerotic plaque that results in a platelet aggregation reaction in the coronary artery. The administration of antiplatelet agents starting from the acute phase of the disease has helped reduce the risk of ischemic relapse both during initial and long-term hospitalization. Management of clopidogrel following an ischemic event has been the subject of several treatment regimens ranging from a single continuous dose to a sequential double dose of between 7 and 30 days. The CURRENT-OASIS 7 therapeutic trial showed a benefit of clopidogrel double dose in reducing the risk of myocardial intervention (MI) and the composite outcome: cardiovascular mortality, MI, or stroke (CVA/TIA) at 30 days. However, the study protocol was interested in all ACSs, regardless of the Type 2 Diabetes Mellitus (T2DM) status in selected patients. Also, doubling of clopidogrel dose was maintained over 7 days after angioplasty. The literature describes an increased cardiovascular risk in type II diabetics in secondary prevention. No previous study has evaluated the effect of clopidogrel double dose given for 1 month on the reduction of this risk in the long-term in diabetic patients. Thus, the objective of this study is to evaluate the efficacy and safety of clopidogrel double dose, given for 1 month in ACS in the diabetic patient.

NCT ID: NCT01148147 Completed - Clinical trials for Coronary Angioplasty

Intracoronary Adenosine Administration to Prevent Periprocedural Myonecrosis in Elective Coronary Angioplasty

PREVENT-ICARUS
Start date: November 2009
Phase: Phase 3
Study type: Interventional

Aim of the study is to evaluate the benefits from adjunctive intracoronary administration of adenosin in elective patients undergoing coronary angioplasty.

NCT ID: NCT00372671 Completed - Clinical trials for Myocardial Infarction

Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

Start date: June 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether a pre-discharge videotape introducing the concept and benefit of a Cardiac Rehabiliation & Secondary Prevention (CRSP) program will increase intent to participate in a CRSP program in post myocardial infarction, unstable angina, coronary artery bypass surgery, or coronary angioplasty patients.

NCT ID: NCT00264264 Completed - Clinical trials for Coronary Artery Disease

Arterial Closure vs Direct Compression for Hemostasis After PCI - The ACDC Trial

Start date: July 2006
Phase: N/A
Study type: Interventional

Hemostasis at the arterial puncture site after percutaneous coronary interventions is achieved by either placement of a puncture closure device or by delaying sheath removal for hours to allow normalization of heparin induced anticoagulation. Both of these methods are far from ideal. Delayed sheath removal poses a risk of recurrent bleeding, hematoma formation and results in decreased patient mobility while the safety of closure devices has been called into question by several recent reports. Due to the lack of definitive data, the arterial access site management varies considerably between physicians and among institutions. The proposed study will evaluate the safety and efficacy of arterial closure devices to achieve hemostasis compared with immediate sheath removal after protamine administration followed by direct compression after percutaneous coronary intervention procedures.