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NCT ID: NCT00720720 Withdrawn - Clinical trials for Hypercholesterolemia

Effect of Phytosterols Enriched Products Consumption on Carotid Artery Artherosclerotic Plaque

PHYTOPLAQUES
Start date: December 16, 2009
Phase: N/A
Study type: Interventional

The objective of this exploratory study is to analyse in humans any qualitative changes of carotid artery atherosclerotic plaque under the influence of plant sterols consumption.

NCT ID: NCT00713947 Withdrawn - Coronary Thrombosis Clinical Trials

Effectiveness of the Eradication of Helicobacter Pylori and an Inhibitor of Pump With Proton Versus Control

Aspylori
Start date: April 2008
Phase: Phase 4
Study type: Interventional

Low dose of aspirin is the main cause of gastro-duodenal ulcer. The best prevention is not definite particularly in patients without history of ulcer and infected by H. pylori.The aim of the study is to evaluate the gastric damage induced by aspirin in patients with H. pylori infection but who have any history of ulcer.

NCT ID: NCT00579046 Withdrawn - Clinical trials for Chronic Obstructive Pulmonary Disease

Study of Erythropoietin to Treat Anemia Complicating Chronic Obstructive Pulmonary Disease

ELAB
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the impact of erythropoietin treatment of anemia on exercise capacity of patients with chronic obstructive pulmonary disease (COPD).

NCT ID: NCT00415155 Withdrawn - Clinical trials for Hepatocellular Carcinoma

A Study of LY2181308 in Patients With Advanced Hepatocellular Carcinoma

Start date: August 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of this study is to estimate the time to progressive disease for patients with advanced hepatocellular cancer who receive LY2181308.

NCT ID: NCT00382837 Withdrawn - Clinical trials for Systemic Lupus Erythematosus

Study of Epratuzumab in Systemic Lupus Erythematosus

Start date: January 2007
Phase: Phase 3
Study type: Interventional

Epratuzumab is an investigational antibody designed to help treat SLE. The purpose is to evaluate safety and long term efficacy in concert with standard SLE treatments

NCT ID: NCT00298467 Withdrawn - Clinical trials for Lymphoma, Large-Cell

MDX-060 in Patients With Relapsed or Refractory Classic Systemic or Primary Cutaneous Anaplastic Large Cell Lymphoma

Start date: February 2006
Phase: Phase 2
Study type: Interventional

This study is an open-label, fixed-dose, multicenter study of MDX-060 in patients with ALCL who have relapsed or refractory disease. There will be 3 phases of this study: Induction, Maintenance, and Follow-up. Patients will be required to attend all protocol-required visits in the 4-week Induction Phase, in which administration of MDX-060 will occur, as well as other testing. Patients who complete the Induction Phase may be eligible for additional MDX-060 treatment ever 2 months for 1 year in the Maintenance Phase. Patients who complete the Maintenance Phase with a response of stable disease or better will be followed every 2 months for 1 year or until disease progression. The purpose of this study is to determine objective response rate at Day 50 in patients with relapsed or refractory classic systemic ALCL or primary cutaneous ALCL treated with MDX-060. Other objectives will be evaluated.

NCT ID: NCT00213356 Withdrawn - Clinical trials for Spinal Cord Injuries

Study of the Nervous Control of the Anal Sphincter

Start date: April 2003
Phase: N/A
Study type: Observational

Anal incontinence and constipation are frequently observed in patients with neurological disease. The purpose of this study is to evaluate the neurological control of the anal sphincter in healthy subjects, patients with neurological disease by a new electrophysiological technique. This technique consists in recordings of anal sphincter responses after magnetic stimulations of the cortex and the sacral nerves.

NCT ID: NCT00213330 Withdrawn - Ulcerative Colitis Clinical Trials

Cerebral Resonance Magnetic Imaging During Rectal Distention

Start date: April 2003
Phase: N/A
Study type: Observational

Irritable bowel syndrome is responsible for chronic abdominal pain, diarrhea and/or constipation. It is a very frequent problem. However, the exact cause of irritable bowel syndrome remains unknown. The purpose of this study is to look for a different cerebral response by magnetic resonance imaging after rectal stimulation in patients with irritable bowel syndrome compared to healthy subjects and to patients with digestive organic disease. Our hypothesis is that irritable bowel syndrome could be a problem of cerebral integration of visceral stimulation.

NCT ID: NCT00168051 Withdrawn - Hemophilia A Clinical Trials

Study Comparing Blood Levels of ReFacto and Advante in Hemophilia A

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

The purpose of the study is to compare the pharmacokinetic parameters of ReFacto and Advate, using the chromogenetic substrate assay to measure plasma Factor VIII activity in plasma.

NCT ID: NCT00151385 Withdrawn - Hemophilia A Clinical Trials

Study Evaluating Inhibitor Specificity in Hemophilia A

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

This investigation will utilize a systematic determination of anti-FVIII antibody specificity in PTPs (> 50 ED) with hemophilia A who have developed inhibitors in response to treatment with any FVIII product(s). A group of patients with hemophilia A, who have no evidence of current or prior FVIII inhibitor will be included for comparison. The objective of this study is to describe the patterns of antibodies and associated epitopes in the study population.