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NCT ID: NCT00501176 Completed - Pancreas Cancer Clinical Trials

Preoperative Stent Study

Start date: December 2006
Phase: N/A
Study type: Interventional

Randomized study comparing the effect of plastic stents to that of expandable metal stents as pre-operative drainage of the bile ducts prior to Whipple operation.

NCT ID: NCT00500968 Completed - Pancreas Cancer Clinical Trials

Study Assessing the Effect of Transpapillary Pancreas Duct Stent in Resection of the Pancreatic Tail

Start date: November 2006
Phase: N/A
Study type: Interventional

Randomized study assessing the effect of transpapillary pancreas duct stent in resection of the pancreatic tail.

NCT ID: NCT00500266 Completed - Clinical trials for Pneumococcal Infections

Study Evaluating Safety of 13-Valent Pneumococcal Conjugate Vaccine in Healthy Elderly Subjects

Start date: May 2008
Phase: Phase 3
Study type: Interventional

To evaluate the safety of 13-valent pneumococcal conjugate vaccine (13vPnC) in elderly subjects who were vaccinated with one or more doses of 23-valent pneumococcal polysaccharide vaccine (23vPS) at least 3 years before study enrollment.

NCT ID: NCT00499200 Completed - Alzheimer's Disease Clinical Trials

Study Evaluating Safety, Tolerability, Pharmacokinetics and 5 HT1A Receptor Occupancy

Start date: October 2007
Phase: Phase 1
Study type: Interventional

The study will include a preliminary pharmacokinetics (PK) / safety / tolerability evaluation in healthy elderly subjects followed by the Receptor Occupancy (RO) evaluations in healthy elderly subjects and in Alzheimer's Disease (AD) subjects.

NCT ID: NCT00498836 Completed - Malignant Melanoma Clinical Trials

Multicentre, Dose Finding, Ph II,CP-4055 in Comb. With Sorafenib - Patients With Metastatic Malignant Melanoma

Start date: March 2007
Phase: Phase 2
Study type: Interventional

Patients with metastatic malignant melanoma will receive CP-4055 200 mg/m2/day intravenously (IV) on Day 1-5 every four weeks and sorafenib 400 mg b.i.d. (twice daily) every day until complete response or disease worsening/progressing.

NCT ID: NCT00498797 Completed - Prostate Cancer Clinical Trials

E3-Hormone Refractory Prostrate Cancer Taxotere Combination

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

The purpose of this study is to determine whether treatment with Zactima (vandetanib) in combination with Docetaxel and Prednisolone is more effective than the standard Docetaxel and Prednisolone alone for prostate cancer, in patients with Hormone refractory prostate cancer who have not previously received chemotherapy.

NCT ID: NCT00496769 Completed - Atrial Fibrillation Clinical Trials

A Phase III Study of Apixaban in Patients With Atrial Fibrillation

AVERROES
Start date: August 31, 2007
Phase: Phase 3
Study type: Interventional

The purpose of this clinical research study is to determine whether apixaban is more effective than acetylsalicylic acid in the prevention of strokes associated with patients with atrial fibrillation. The safety of this treatment will also be studied.

NCT ID: NCT00496470 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease, COPD

Evaluation of Efficacy and Safety of Symbicort® as an add-on Treatment to Spiriva® in Patients With Severe COPD.

Start date: May 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the effect of combined treatment with Symbicort and Spiriva, in terms of improvement of lung function, symptoms and inflammatory markers, in patients with severe COPD.

NCT ID: NCT00494949 Completed - Hypotension Clinical Trials

Increasing Dose Safety Study of Hemospan in Orthopedic Surgery Patients

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

The purpose of this study is to evaluate the safety and possible effectiveness of Hemospan solution in patients undergoing elective orthopedic surgery who receive spinal anesthesia.

NCT ID: NCT00494793 Completed - Open Abdomen Clinical Trials

Vacuum Assisted Wound Closure (VAWC) and Mesh Mediated Fascial Traction

Start date: April 1, 2006
Phase: N/A
Study type: Interventional

The purpose of this multicenter trial is to prospectively evaluate a novel combination of vacuum assisted wound closure (VAWC) and mesh mediated fascial traction for closure of open abdomens.