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NCT ID: NCT00922519 Terminated - Bone Scan Clinical Trials

Observational Pilot Study of 18F-Sodium Fluoride (Na18F) Whole Body Positron Emission Tomography (PET) Scans for Imaging Bone

Start date: June 18, 2009
Phase:
Study type: Observational

This study is being done to provide an alternative to bone scanning with technetium-99m (99mTc) labelled diphosphonates, and to document the safety of {18F}-Sodium Fluoride (Na18F) as a Positron Emission Tomography (PET) imaging radiopharmaceutical. Since the current availability of 99mTc was severely reduced because of the Chalk River shut down, alternative approaches to done scanning are needed. PET imaging with Na18F is one alternative approach to providing this critical clinical service.

NCT ID: NCT00919945 Terminated - Clinical trials for Congenital Heart Disease

Impact of Early Enteral Feeding on Splanchnic Blood Flow After Surgery for Critical Heart Disease in the Newborn

Start date: January 2009
Phase: Phase 2
Study type: Interventional

The objective of this study is to determine the impact of early post-operative feeding on splanchnic blood flow, cardiac output and end organ perfusion, and the patients overall clinical outcomes.

NCT ID: NCT00917293 Terminated - Tardive Dyskinesia Clinical Trials

Safety and Efficacy of Pyridoxal 5' -Phosphate in the Treatment of Tardive Dyskinesia

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The primary objective is to assess the safety and effectiveness of Pyridoxal 5'-Phosphate on the reduction of expressed symptoms of tardive dyskinesia in patients with schizophrenia and schizoaffective disorders.

NCT ID: NCT00912288 Terminated - Alzheimer Disease Clinical Trials

A Phase 3 Efficacy Study Of Dimebon In Patients With Moderate To Severe Alzheimer's Disease

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

No Dimebon clinical data exist yet in patients with disease that has advanced to the moderate-to-severe stage. Therefore, this study evaluates the safety and efficacy of Dimebon in patients with moderate-to-severe AD who are receiving existing background therapy with memantine.

NCT ID: NCT00908024 Terminated - Colorectal Cancer Clinical Trials

Combination Study of BMS-754807 and Erbitux® in Subjects With Advanced or Metastatic Solid Tumors

Start date: October 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The study is expected to identify a safe dose of BMS-754807 to be given in combination with a standard dose of cetuximab and the recommended dose or dose range for Phase II studies. The study is also intended to collect first data on the effects of the combination of BMS-754807 with cetuximab on tumors of patients with colorectal cancer or squamous cell cancer of the head and neck for whom cetuximab-containing therapies have not been effective

NCT ID: NCT00904137 Terminated - Clinical trials for Type I Supracondylar Fracture of the Humerus

Treatment of Type I Supracondylar Fractures of the Humerus

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

Type I supracondylar fractures are elbow fractures that occur in children aged 3-10 years. Many different treatment options exist to treat this type of fracture. The purpose of this study is to compare three different treatment modalities with regards to pain experienced during treatment, the amount of pain medication needed during treatment, and any short-term complications. We hypothesize that above elbow casting and long-arm splinting will result in less pain and have fewer complications than taping the elbow in flexion.

NCT ID: NCT00902863 Terminated - Chronic Pain Clinical Trials

Impact of a Course on Stress Reduction

YOGA
Start date: February 2009
Phase: N/A
Study type: Interventional

This project seeks to measure the effectiveness of a course in self-management strategies (including yoga, mindfulness, and breathing exercises). The course will be provided by a certified yoga instructor to patients being followed at the Pain Management Centre, Hamilton Health Sciences (HHS).

NCT ID: NCT00901160 Terminated - Blood Clotting Clinical Trials

Thromboelastography (TEG®) and Platelet Function in Patients on Anti-platelet Agents

Start date: January 2008
Phase: Phase 1
Study type: Observational

Can a post-operative analysis using a simple blood test (Thromboelastography(TEG®)) and Platelet Mapping Assay (PMA™) be able to detect the occurence of clotting or bleeding complications in patients on blood thinning (anti-platelet) agents?

NCT ID: NCT00901108 Terminated - Open Angle Glaucoma Clinical Trials

Trabectome Versus Trabeculectomy With Mitomycin C in Patients With Open Angle Glaucoma

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

The purpose of this study is to compare the efficacy and safety of Trabectome versus Trabeculectomy with adjunctive Mitomycin C, combined with cataract surgery, in patients with open angle glaucoma.

NCT ID: NCT00900549 Terminated - Heart Failure Clinical Trials

Evaluation of Resynchronization Therapy for Heart Failure

EARTH
Start date: October 2003
Phase: Phase 4
Study type: Interventional

Heart failure is a major health problem in Canada. Recent advances in medical and device therapy have helped to reduce the morbidity and mortality of patients with this problem. Among these treatments, cardiac resynchronization therapy (CRT) has very recently been shown to be effective to improve functional class, quality of life and exercise tolerance of the patients with the most severe symptoms of heart failure and a prolonged duration of the QRS on the 12-lead Electrocardiography (ECG).