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NCT ID: NCT00509145 Completed - Multiple Sclerosis Clinical Trials

Safety and Efficacy of Orally Administered Laquinimod Versus Placebo for Treatment of Relapsing Remitting Multiple Sclerosis (RRMS)

ALLEGRO
Start date: November 13, 2007
Phase: Phase 3
Study type: Interventional

Determination the efficacy of daily oral treatment with laquinimod 0.6 mg capsules as compared to placebo in subjects with Relapsing Remitting Multiple Sclerosis (RRMS).

NCT ID: NCT00509054 Completed - Parastomal Hernia Clinical Trials

Prevention of Parastomal Hernia With a Mesh

Start date: January 2001
Phase: Phase 4
Study type: Interventional

Parastomal hernias are randomised to either a conventional stoma formed through the rectus anterior muscle or to the same procedure with the addition of a prophylactic mesh in a sublay position.

NCT ID: NCT00508053 Completed - Wound Infection Clinical Trials

When Closing Midline Incisions, do Small Stitches Reduce the Risk for Incisional Hernia, Wound Infection or Dehiscence?

Start date: January 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a technique using very small stitches when closing a midline incision can reduce the risk for wound complications such as incisional hernia, infection or dehiscence.

NCT ID: NCT00505388 Completed - Bronchial Asthma Clinical Trials

A Follow-up Programme for Patients Using Symbicort SMART in Normal Clinical Practice

Start date: July 2007
Phase:
Study type: Observational

This patient follow-up programme was designed to describe the extent of Symbicort use in patients prescribed Symbicort as maintenance and reliever therapy in routine clinical practice in comparison with the already documented use of Symbicort as maintenance and reliever therapy in clinical therapies

NCT ID: NCT00504881 Completed - Epilepsy Clinical Trials

Brivaracetam as add-on Treatment in Adolescents and Adults Suffering From Epilepsy

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

This study will compare the safety and efficacy of Brivaracetam at flexible dose with Placebo in subjects suffering from Epilepsy.

NCT ID: NCT00501969 Completed - Clinical trials for Advanced Stage Parkinson's Disease

An Open-Label Extension Trial to Assess the Safety of Long-Term Treatment of Rotigotine in Advanced-Stage Parkinson's Disease

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

The objective of this open-label extension is to assess the safety and tolerability of long-term treatment of the rotigotine patch in subjects with advanced-stage idiopathic Parkinson's disease

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.