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NCT ID: NCT00862888 Completed - Clinical trials for Erectile Dysfunction

Study to Investigate Effect of a New Drug (PF-00446687) in Males Suffering From Erectile Dysfunction

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

The purpose of this study is to investigate the effect of up to 200 mg of PF-00446687 on erectile activity in males suffering from erectile dysfunction as well as examining the safety and toleration of the drug.

NCT ID: NCT00862147 Terminated - Child Development Clinical Trials

Effectiveness Study of the International Child Development Program

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

The objective of this study is to evaluate the effect of the International Child Development Program (ICDP). Research questions to be answered: 1. Does the ICDP affect children's psychosocial functioning compared to treatment as usual? 2. Does the ICDP change parent-child interaction?

NCT ID: NCT00860288 Completed - Clinical trials for Diabetes Mellitus, Type 2

Efficacy and Long-Term Safety of Vildagliptin as Add-on Therapy to Metformin in Patients With Type 2 Diabetes

Start date: February 2009
Phase: Phase 2/Phase 3
Study type: Interventional

This is a 2-3 period parallel group study with an adaptive element in Type 2 diabetes patients receiving vildagliptin as add-on therapy to metformin

NCT ID: NCT00860236 Completed - Clinical trials for Chronic Fatigue Syndrome

Giardia Induced Fatigue and Functional Gastrointestinal Diseases

GIFF
Start date: March 2009
Phase: Phase 4
Study type: Interventional

A giardiasis outbreak in Bergen has given us the opportunity to approach two basic research questions of national and global importance: - Studying the pathoimmunology of giardiasis in a natural setting, and following the genetic and immunological responses leading to recovery or persistent disease and sequelae. - Studying the two disease entities FGID and CFS when induced by acute giardiasi and their risk factors. - Interventional cognitive behavioural therapy is the only intervention documented to have significant effect on CFS outcome, and conventional cognitive behavioural therapy will be compared to a psycho-educational programme in the format of a randomised controlled trial.

NCT ID: NCT00858780 Completed - Clinical trials for Rheumatoid Arthritis

Study Comparing The Effect On Disease Activity When Reducing Or Discontinuing Etanercept In Subjects With RA

DOSERA
Start date: January 2009
Phase: Phase 4
Study type: Interventional

This study involves Rheumatoid Arthritis patients in regular clinical setting who are already on etanercept treatment and are in remission or in a low disease activity (LDA) state, and is intended to identify parameters that can serve as guidance in clinical settings. This study will consider the clinical and radiographic course in subjects when etanercept treatment is tapered or discontinued, and analyze the subjects' experience of disease worsening and the predictive values of clinical parameters, serum biomarkers and imaging on the clinical and radiographic course in different treatment groups. The effect of re-treatment with etanercept at treatment failure will also be studied.

NCT ID: NCT00857129 Completed - Clinical trials for Low Risk Birth; Births With Low Risk Factor

Can Differentiated Birth Care Improve the Service?

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

Prospective evaluation of birth complication in three differently staffed and equipped units in the same hospital.

NCT ID: NCT00857103 Completed - Lymphoma Clinical Trials

Effect of Interactive Tailored Assessment on Patient-provider Communication

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

This interdisciplinary international research collaboration will test effects of Choice, a computer-assisted, interactive support system designed to help cancer patients communicate their symptoms and preferences, and clinicians in incorporating this information into patient care. In this pretest-post test clinical trial with 200 leukemia and lymphoma patients we will: 1) Test effects of Choice when integrated into routine clinical practice on: patient-provider communication, documented patient care, anxiety and patient satisfaction; 2) analyze relationships among the above variables and explore differences in these relationships between groups; 3) analyze group differences in communication style in terms of instrumental and affective behavior, content, participation, initiative and person addressed; and 4) investigate the extent of the time requirements when using Choice in clinical practice, perceived usefulness and ease of use.

NCT ID: NCT00856661 Terminated - Stroke Clinical Trials

Efficacy and Safety Study of Desmoteplase to Treat Acute Ischemic Stroke (DIAS-4)

Start date: April 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine whether desmoteplase is effective and safe in the treatment of patients with acute ischaemic stroke when given within 3 to 9 hours from onset of stroke symptoms.

NCT ID: NCT00856076 Recruiting - Clinical trials for Venous Thromboembolism

Venous Thromboembolism in Pregnancy Study

VIP
Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is to investigate clinical, biochemical and genetic risk factors for venous thromboembolism in pregnancy and pregnancy related vascular complications, and the long-term outcome of such complications including implications for quality of life.

NCT ID: NCT00855621 Active, not recruiting - Parkinson's Disease Clinical Trials

Effects of Deep Brain Stimulation in Parkinson's Disease

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to identify factors predicting good results in patients treated with deep brain stimulation for Parkinson's disease. The study includes a comparison of two surgical methods used to provide this therapy.