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NCT ID: NCT00367315 Completed - Knee Osteoarthritis Clinical Trials

Efficacy and Safety of Lumiracoxib in Patients With Primary Knee Osteoarthritis (OA)

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

This study will evaluate the efficacy and safety of using lumiracoxib in the treatment of patients with knee osteoarthritis (OA)

NCT ID: NCT00366249 Completed - Diabetic Foot Clinical Trials

Study Evaluating the Safety and Efficacy of a Once-daily Dose of Tigecycline vs Ertapenem in Diabetic Foot Infections (DFI) With a Substudy in Patients With Diabetic Foot Infections Complicated by Osteomyelitis.

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

The purpose of this study was to look at the safety and effectiveness of a once-daily dose of tigecycline compared to ertapenem for the treatment of diabetic foot infections. The co-primary efficacy endpoints were not met.

NCT ID: NCT00366145 Completed - Clinical trials for Graft Versus Host Disease

Efficacy and Safety of Adult Human Mesenchymal Stem Cells to Treat Steroid Refractory Acute Graft Versus Host Disease (GVHD)

Start date: August 17, 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and gather additional safety information for Prochymal® in participants who have failed to respond to steroid treatment of Grades B-D acute GVHD.

NCT ID: NCT00362661 Terminated - Clinical trials for Posttraumatic Stress Disorder

Low-dose Cortisol in Chronic Posttraumatic Stress Disorder

Start date: June 2007
Phase: N/A
Study type: Interventional

The aim of this prospective, double-blind, placebo-controlled, cross-over study is to determine the therapeutic efficacy of low-dose cortisol for symptoms of chronic posttraumatic stress disorder.

NCT ID: NCT00362609 Completed - Clinical trials for Gastroesophageal Reflux

Study Evaluating Pantoprazole in Neonates and Preterm Infants With GERD

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

The purpose of this study is to determine whether or not consistent drug levels can be achieved in infants with presumed Gastroesophageal Reflux Disease.

NCT ID: NCT00360178 Completed - Hypertension Clinical Trials

Efficacy and Safety of Valsartan Plus Hydrochlorothiazide in Fixed Dose Combination in Hypertensive Patients Not Controlled by the Free Combination of an Angiotensin Receptor Blocker Plus Hydrochlorothiazide

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

Recruiting in Germany only: This study will evaluate the safety and efficacy of valsartan plus HCTZ in fixed dose combination in hypertensive patients not responding to treatment with the free combination of Candesartan plus HCTZ. In an optional extension patients with uncontrolled BP at the end of the core study can be treated with valsartan plus HCTZ in fixed dose combination plus amlodipine 5 mg for additional 4 weeks.

NCT ID: NCT00359762 Completed - Clinical trials for Type 2 Diabetes Mellitus

Exenatide Versus Glimepiride in Patients With Type 2 Diabetes

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This study assesses the effects of twice-daily subcutaneous injection exenatide versus treatment with sulfonylurea (glimepiride) on long-term glycemic control and beta-cell function.

NCT ID: NCT00359424 Terminated - Stroke Clinical Trials

Interventional Management of Stroke (IMS) III Trial

IMSIII
Start date: August 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare two different treatment approaches to recanalization started within 3 hours of symptom onset—combined intravenous (IV) and endovascular therapy and standard intravenous (IV) rt-PA alone.

NCT ID: NCT00359112 Completed - Clinical trials for Non-Insulin-Dependent Diabetes Mellitus

AVANDAMET Versus Metformin And Sulphonylurea In People With Poorly Controlled Type 2 Diabetes

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

This study compares the effects of Avandamet (rosiglitazone maleate/metformin) treatment and metformin plus sulphonylurea treatment in overweight people with type 2 diabetes.

NCT ID: NCT00358956 Completed - Thyroid Cancer Clinical Trials

A Study To Assess ZD6474 (ZACTIMAâ„¢) Monotherapy In Locally Advanced or Metastatic Hereditary Medullary Thyroid Cancer

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

This will be a Phase II, open label study to establish the effect of once-daily oral doses of ZD6474 100mg in subjects with locally advanced or metastatic hereditary medullary thyroid cancer in whom no standard therapeutic option is available.