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NCT ID: NCT00225511 Completed - Depression Clinical Trials

Study Evaluating Effexor XR for Major Depression.

Start date: June 2004
Phase: Phase 3
Study type: Interventional

Study Evaluating Effexor XR for Major Depression.

NCT ID: NCT00225485 Completed - Depression Clinical Trials

Study Evaluating Effexor XR in Elderly Patients With Major Depression.

Start date: December 2003
Phase: Phase 3
Study type: Interventional

Phase III study evaluating Effexor XR in elderly patients with major depression.

NCT ID: NCT00221156 Completed - Clinical trials for Coronary Artery Disease

Acarbose and Secondary Prevention After Coronary Stenting

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

The purpose of this study is to determine whether the intervention for newly diagnosed abnormal glucose tolerance after coronary stenting will improve the long-term clinical outcome.

NCT ID: NCT00221143 Completed - Ischemia Clinical Trials

Stem Cell Study for Patients With Leg Ulcer/Gangrene

Start date: November 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if stem cell therapy with one's own cells (autologous cells) delivered intramuscularly to one's leg with ulcer and/or gangrene due to poor blood flow will be safe and if it will relieve leg pain, increase blood flow, and/or cure the leg wound.

NCT ID: NCT00221130 Completed - Adult Periodontitis Clinical Trials

Clinical Trials of Regeneration for Periodontal Tissue

Start date: July 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Adult periodontitis is a chronic infective disease affecting the periodontium. Periodontitis induce the destruction of attachment apparatus of teeth, resulting in periodontal pocket formation and teeth loss. This study will test the safety and efficacy of alveolous bone reproduction by the transplantation of mixture named periodontium injectable gel for the adult periodontitis patients. Injectable gel is the mixture of ex-vivo cultured mesenchymal stem stem cells, ex-vivo cultured osteoblast-like cells differentiated from mesenchymal stem cells and scaffold (include, platelet rich plasma, human thrombin and calcium chloride).

NCT ID: NCT00221104 Completed - Ischemic Stroke Clinical Trials

Japan Statin Treatment Against Recurrent Stroke (J-STARS)

Start date: March 1, 2004
Phase: Phase 3
Study type: Interventional

Although hyperlipidemia is not always the risk factor of stroke, inhibition of 3-hydroxy-3-methylglutaryl-coenzyme A(HMG-CoA) reductase can decrease the incidence of stroke in the patient with ischemic heart disease. The neuroprotective mechanism beyond cholesterol lowering should be expected to attenuate inflammation and atherosclerosis. The present study hypothesizes if pravastatin prevents recurrent stroke in the ischemic stroke patients with safety.

NCT ID: NCT00221091 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus

Study to Evaluate Efficacy of Shunt Operation for Idiopathic Normal Pressure Hydrocephalus

Start date: September 2004
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy of shunt operation for idiopathic normal pressure hydrocephalus, and determines the diagnostic value of noninvasive procedures commonly practiced in the clinic.

NCT ID: NCT00220285 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Study for Evaluation of Efficacy and Safety of SH L 749 to Indolent B-cell Non-Hodgkin's Lymphoma

Start date: August 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the antitumor effect and safety of the product for relapsed or refractory indolent B-cell non-Hodgkin's lymphomas.

NCT ID: NCT00219427 Completed - Vision, Low Clinical Trials

Retina Projection System Trials for Low Vision People

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

1. Purpose a. Examination on Efficacy of Retina Projection System 2. Patients a. Low vision patients 3. Methods 1. Vision aids - Retina Projection System - Face-mounted video display as control 2. Comparison of Reading Speeds with both vision aids

NCT ID: NCT00219375 Completed - Acute Lung Injury Clinical Trials

Study of Sivelestat Sodium Hydrate in Acute Lung Injury (ALI) Associated With Systemic Inflammatory Response Syndrome (SIRS) in Japan

Start date: June 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to confirm the efficacy and safety of sivelestat in patients with acute lung injury associated with systemic inflammatory response syndrome. The results will be compared to the study with conventional treatment without sivelestat.