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Coronary Disease clinical trials

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NCT ID: NCT00248066 Completed - Clinical trials for Coronary Artery Disease

Safety and Efficacy of RESTEN-MP When Used in Conjunction With a Bare Metal Stent in Coronary Arteries

Start date: September 2005
Phase: Phase 2
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 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 and potential effectiveness of RESTEN-MP to reduce in-stent restenosis following balloon angioplasty and stent placement. The post-dose follow-up period is up to six-months. RESTEN-MP is administered at the time a stent is successfully placed in a coronary artery, and again 24 hours later, via slow-push intravenous administration.

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: 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: NCT00242944 Completed - Clinical trials for Hypercholesterolemia

Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome (JAPAN-ACS)

Start date: November 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effects of pitavastatin and atorvastatin on coronary plaque volume in patients with acute coronary syndrome and to clarify the relationship between coronary plaque volume, serum lipids, and inflammation markers in order to determine the significance of intensive lipid lowering therapy in patients with acute coronary syndrome in Japan.

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.