Clinical Trials Logo

Filter by:
NCT ID: NCT00224497 Completed - Alzheimer's Disease Clinical Trials

A Dose Ranging Study To Investigate The Efficacy And Safety Of SB-742457 In Alzheimer's Disease

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

The purpose of this study is to find out if SB-742457 is a safe treatment and what effects it has on the symptoms of mild to moderate Alzheimer's disease. SB-742457 is a new treatment which is thought to increase the levels of certain chemicals in the brain that are often decreased in patients with Alzheimer's disease.

NCT ID: NCT00223977 Completed - Clinical trials for Iron Deficiency Anemia

2 Doses of Ferrlecit Versus Oral Iron to Treat Iron-deficiency Anemia in Peritoneal Dialysis Patients.

Start date: December 2003
Phase: Phase 2/Phase 3
Study type: Interventional

This is a phase 3 clinical investigation. Patients who meet the eligibility criteria and provide signed informed consent will be randomized to receive one of two levels of Ferrlecit or oral iron in a 1:1:1 ratio.

NCT ID: NCT00223964 Completed - Anemia Clinical Trials

Study of the Efficacy of Two Doses of Ferrlecit in the Treatment of Iron Deficiency in Pediatric Hemodialysis Patients

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

This was a multi-center study in iron-deficient pediatric hemodialysis patients, whose legal guardian had provided signed informed consent and satisfied the inclusion and exclusion criteria.

NCT ID: NCT00219973 Completed - Cancer Clinical Trials

CANBESURE STUDY (Cancer, Bemiparin and Surgery Evaluation)

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

The aim of the study is to evaluate the efficacy and safety of Bemiparin, a second-generation LMWH, in the prophylaxis of VTE (using a postoperative regimen, i.e. administering the first dose 6 hours after finishing the surgical procedure) for 28 days compared to 8 days, in oncological surgery.

NCT ID: NCT00219141 Completed - Hypertension Clinical Trials

Aliskiren in Combination With Losartan Compared to Losartan on the Regression of Left Ventricular Hypertrophy in Overweight Patients With Essential Hypertension

ALLAY
Start date: October 2005
Phase: Phase 3
Study type: Interventional

To compare the efficacy and safety of aliskiren in combination with losartan compared to losartan on the regression of the increased size of the left ventricle in overweight patients with high blood pressure.

NCT ID: NCT00218673 Completed - HIV Infections Clinical Trials

RCT of Russian IDU Peer Network HIV Prevention Intervention - 1

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

The purpose of this study is to conduct a randomized controlled trial to assess the efficacy of a peer-educator intervention focused on injection drug users and their drug and sexual networks. We expect that participants who receive the intervention will demonstrate a reduction in the rate of HIV infection and HIV risk behaviors and members of their risk network will also demonstrate reductions in risk behaviors compared to those in the control group.

NCT ID: NCT00218426 Completed - Clinical trials for Opioid-Related Disorders

Addiction Treatment in Russia: Oral vs. Naltrexone Implant

Start date: July 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Heroin addiction is a growing problem in Russia; individuals who enter heroin addiction treatment often relapse. Therefore, effective heroin addiction treatments are necessary to prevent relapse. The purpose of this study is to compare oral naltrexone with a naltrexone implant that provides opioid blockade for two months in preventing relapse to heroin addiction in St. Petersburg, Russia.

NCT ID: NCT00216619 Completed - Migraine Clinical Trials

The Prolonged Use of Topiramate for Preventing Migraine Headaches

PROMPT
Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness (beyond 6 months) of individualized doses (100 to 200 milligrams) of topiramate for the prevention of migraine headaches over a period of 26 weeks.

NCT ID: NCT00215683 Completed - Prostate Cancer Clinical Trials

An Extension Study Evaluating the Long-Term Safety and Tolerability of Degarelix One-Month Depots in Prostate Cancer

Start date: February 2005
Phase: Phase 2/Phase 3
Study type: Interventional

This was an extension study for the study FE200486 CS12 (NCT00819156). Each participant was to be treated until he was discontinued or withdrawn from the study, or a marketing authorization for degarelix had been obtained. The study was terminated when all ongoing participants had been treated for at least 5 years (including one year in the main study).

NCT ID: NCT00210431 Completed - Cerebral Palsy Clinical Trials

Post Marketing Surveillance Study of Dysport

Start date: October 2004
Phase:
Study type: Observational

The purpose of this study is to provide further information regarding the risks and benefits of Dysport in marketed indications.