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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00245401 Completed - Clinical trials for Coronary Artery Disease

CYPHERTM Stent Post-Marketing Surveillance Registry (US-PMS)

Start date: August 2003
Phase: Phase 4
Study type: Interventional

The purpose of this PMS registry, named e-CYPHER Stent Registry, is to collect post marketing surveillance data on the CYPHERTM Sirolimus-eluting Coronary Stent following marketing approval, when used in normal clinical practice within the labeled indications.

NCT ID: NCT00245284 Completed - Clinical trials for Coronary Artery Disease

Predictor of Advanced Subclinical Atherosclerosis

Start date: September 2005
Phase: N/A
Study type: Observational

Evaluation of skin cholesterol for cardiovascular risk assessment in asymptomatic individuals at low, intermediate, or high risk based on Framingham Global Risk estimates. Carotid intima-media thickness (IMT), a surrogate marker for atherosclerotic burden, that independently predicts the occurrence of heart attack and stroke, will be the “gold standard” comparator. Hypothesis: Skin cholesterol, as measured by two non-invasive tests, correlates with CAD, as measured by CIMT in this population.

NCT ID: NCT00244647 Terminated - Clinical trials for Coronary Artery Disease

A Phase 1b Study Evaluating RESTEN-MP in Subjects With Focal de Novo Stenosis

Start date: August 2003
Phase: Phase 1
Study type: Interventional

The process of re-narrowing of a coronary artery following a revascularization procedure such as angioplasty, begins at the time of the procedure. Restenosis has long been considered a major problem for effective long-term interventional success. This often results in repeated procedures to deal with recurrent stenosis (or restenosis) of the original targeted vessel. There is a substantial body of literature suggesting that local MYC protein production in the injured coronary artery is a major stimulus and potential cause of restenosis that appears after stent placement. This study is based upon the hypothesis that stopping MYC protein production in the vessel has will help reduce restenosis (vessel re-narrowing). AVI BioPharma Inc., has utilized its proprietary antisense chemistry to design a drug that interferes with MYC production. This study will evaluate the safety, pharmacokinetics and potential effectiveness of a single intravenous slow-push dose of RESTEN-MP at the time of stent placement to reduce in-stent restenosis following balloon angioplasty and stent placement. The post-dose follow-up period is up to six-months.

NCT ID: NCT00244530 Completed - Clinical trials for Coronary Artery Disease

Prophylactic Effect of Nifedipine on Further Decline in Renal Function in Patients Undergoing Open-Heart Surgery

Start date: June 2001
Phase: Phase 4
Study type: Interventional

To compare renal function (51Cr-EDTA clearance) 48 hours post open-heart surgery (coronary bypass or valve surgery) in patients with impaired renal function after randomization to either nifedipine infusion at start of surgery and the following 24 hours or placebo (0.9% saline infusion). Study hypothesis is that nifedipine has a prophylactic effect on decline in renal function.

NCT ID: NCT00243477 Completed - Clinical trials for Coronary Artery Disease

MOTIV Study- Effect of Antidepressive Treatment by Escitalopram in Patients Undergoing Coronary Artery Bypass Grafting

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of an antidepressive medication (Escitalopram), started preoperatively and given during 6 months, on 6-month and 1 year post-operative morbidity and mortality after coronary artery bypass grafting

NCT ID: NCT00243438 Completed - Coronary Disease Clinical Trials

DaVinci Registry(Distinctly Assess Vision in Coronary Intervention)

Start date: July 2003
Phase: Phase 4
Study type: Observational

Prospective Internet-Registry, Postmarketing-Surveillance, Registration and Follow-up of patients after Multi-Link VISION™ - Stent Implantation

NCT ID: NCT00243308 Terminated - Unstable Angina Clinical Trials

Serp-1 for the Treatment of Acute Coronary Syndrome

Start date: October 2005
Phase: Phase 2
Study type: Interventional

Males and females aged 18-80 years who present with ACS (unstable angina and non ST-elevation MI) defined as one or more episodes of angina lasting at least 5 minutes in the last 24 hours before admission and greater than 0.05 mV of presumed new ST-segment depression in at least 2 contiguous ECG leads OR, angina and per confirmatory angiogram, has been scheduled for percutaneous coronary angioplasty. The primary objective of this study is to evaluate the safety of Serp-1 injection when administered in 3 daily doses to patients undergoing conventional therapy for Acute Coronary Syndrome (ACS) requiring early intervention.

NCT ID: NCT00242697 Completed - Clinical trials for Coronary Artery Disease

Double-Blind Comparison of Combined General-Spinal Anesthesia to General Anesthesia for Coronary Artery Surgery

Start date: April 2002
Phase: Phase 3
Study type: Interventional

Use of neuraxial agents in anesthesia for cardiac surgery is expanding. We have used combined general-spinal anesthesia for cardiac surgery for 12 years. We hypothesized that compared to general anesthesia, the combined techniques would provide comparable intraoperative hemodynamics and improved postoperative analgesia. This study subjected these techniques to a double-blind randomized trial.

NCT ID: NCT00241904 Completed - Hypertension Clinical Trials

Reducing Total Cardiovascular Risk in an Urban Community

COACH
Start date: May 2006
Phase: N/A
Study type: Interventional

PLEASE NOTE: THIS STUDY IS ONLY ENROLLING PATIENTS CURRENTLY BEING TREATED AT BELAIR-EDISON FAMILY HEALTH CENTER. The purpose of this study is to compare the clinical effectiveness and cost effectiveness of two cardiovascular risk reduction programs - a comprehensive intensive (Cl) intervention with a less intensive (LI) intervention - in African American, and white low-income patients with known excessive cardiovascular disease risk.

NCT ID: NCT00241774 Completed - Depression Clinical Trials

Coronary Heart Disease Incidence: Depression & Inflammation Risk

Start date: August 2005
Phase: N/A
Study type: Observational

To examine the associations among depression, inflammation, and coronary heart disease using an existing data base and associated plasma samples.