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NCT ID: NCT00165620 Completed - Lesion Clinical Trials

A Randomized, Open, Parallel, Optimal Injection Rate-Finding Study for E7337 in Dynamic CT of the Liver in Patients With Liver Disease

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

To establish the optimum injection rate for E7337 (Iomeron 350) in dynamic CT in patients who have hepatic lesions.The primary endpoint for efficacy is the contrast enhancement effect in the early arterial phase, and the primary safety endpoints are warming sensation and vascular pain.

NCT ID: NCT00165607 Completed - Osteoporosis Clinical Trials

Randomized, Open, Parallel, Active Controlled Study on Fracture Prevention in Antiosteoporosis Treatment (OF Study)

Start date: April 1996
Phase: Phase 4
Study type: Interventional

To investigate a new incidence and preventive effect of menatetrenone on vertebral fracture in patients with osteoporosis who were randomly assigned to either treatment arm receiving daily dose of calcium supplement as a monotherapy (calcium monotherapy group) or menatetrenone plus calcium supplement as a combination therapy (menatetrenone combo therapy group) for 36 months, followed by a 12-month follow-up observation to examine the preventive effect on the fracture risk.

NCT ID: NCT00165594 Terminated - Gastric Cancer Clinical Trials

A Study of E7070 in Patients With Gastric Cancer

Start date: February 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Phase I study: To investigate primary objective (maximal tolerated dose and dose-limiting toxicity) and secondary objectives (pharmacokinetics, safety, estimation of a recommended dose, and anti-tumor effect by evaluable case) of E7070 in patients with gastric cancer who are extensive or intermediate metabolizer type (EM/IM) to CYP2C9 and CYP2C9 by intravenously administering once every 3 weeks. Phase IIa study: To investigate primary objective (response rate for efficacy assessment) and secondary objectives (frequency and severity of adverse drug reactions, and pharmacokinetics) of E7070 in patient with gastric cancer who are EM/IM type by intravenously administering once every 3 weeks.

NCT ID: NCT00162955 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Prevention of CHOP-induced Chronic Cardiotoxicity

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

The purpose of this study is to assess the protective effect of Valsartan on chronic cardiotoxicity induced by CHOP.

NCT ID: NCT00161369 Completed - Atherosclerosis Clinical Trials

Effect of Homocysteine and Asymmetric Dimethylarginine on Cardiovascular Events in Hemodialysis Patients

Start date: April 2000
Phase: N/A
Study type: Observational

Homocysteine (Hcy) and asymmetric dimethylarginine (ADMA) have recently been recognized as potential risk factors for atherosclerosis in the general population, and the metabolism of each of these substances seems to be closely related. This study investigates the association between these substances, and whether elevated serum levels of Hcy and ADMA would be related to a high risk of atherosclerosis and cardiovascular events in maintenance hemodialysis (HD) patients.

NCT ID: NCT00159913 Completed - Clinical trials for Pulmonary Arterial Hypertension, Children

A Randomized, Double-Blind, Placebo-Controlled Study of Sildenafil in Children With Pulmonary Arterial Hypertension.

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

This is a clinical research study designed to evaluate sildenafil for the treatment of Pulmonary Arterial Hypertension in children, aged 1 to 17 years. The purpose of the study is to assess the efficacy, safety, and pharmacokinetics of 16 weeks of chronic treatment with oral sildenafil given in three different doses, compared to placebo (inactive treatment). Efficacy will be measured by exercise and hemodynamics. Patients who complete this trial may be eligible to take part in an extension study, in which all patients will receive active treatment of sildenafil.

NCT ID: NCT00159874 Completed - Clinical trials for Pulmonary Arterial Hypertension

A Long Term Extension Study Evaluating Safety Of Sildenafil Citrate When Used To Treat Pulmonary Arterial Hypertension (PAH) In Children

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

Active treatment, dose-blinded extension study evaluating the safety and long term efficacy of sildenafil citrate in children with PAH.

NCT ID: NCT00158080 Recruiting - Clinical trials for Chronic Kidney Disease

Hemofiltration for Contrast-Induced Nephropathy

Start date: n/a
Phase: N/A
Study type: Interventional

Contrast-induced acute renal failure can be prevented with hemofiltration which is performed during cardiac catheterization

NCT ID: NCT00154414 Completed - Clinical trials for Diabetes Mellitus, Type 2

Effect of Liraglutide on Blood Glucose Control in Japanese Subjects With Type 2 Diabetes

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

This trial is conducted in Japan. The aim of this research trial is to evaluate the effect of treatment with liraglutide or placebo on blood glucose control after 14 weeks in Japanese subjects with type 2 diabetes. Liraglutide or placebo is administered by injection once daily in the evening. The trial is a multi-national trial with treatment concealed to participating subjects, investigators and the sponsor. Treatment allocation is random with equal chance of being assigned to each group.

NCT ID: NCT00153946 Completed - Stroke Clinical Trials

Edaravone and Argatroban Stroke Therapy Study for Acute Ischemic Stroke

EAST
Start date: August 2004
Phase: Phase 4
Study type: Interventional

Edaravone, a free radical scavenger, is a novel neuroprotective agent, and argatroban is a selective thrombin inhibitor. Both the drugs were approved by the Japanese Government, and have frequently been used for the treatment of acute brain infarction in Japan. The effect of combination therapy of these drugs, however, has not yet been elucidated. This study will test the safety and efficacy of the combination therapy with these agents in patients with acute non-cardioembolic and non-lacunar ischemic stroke.