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NCT ID: NCT01103323 Completed - Clinical trials for Metastatic Colorectal Cancer

Patients With Metastatic Colorectal Cancer Treated With Regorafenib or Placebo After Failure of Standard Therapy

Start date: April 2010
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo-controlled multi-center phase III study to evaluate efficacy and safety of regorafenib in patients with metastatic colorectal cancer (CRC) who have progressed on/after all approved drugs for CRC

NCT ID: NCT01102712 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Bronchoscopic Thermal Vapor Ablation (BTVA) for Lung Volume Reduction

BTVA
Start date: November 2009
Phase: N/A
Study type: Interventional

To establish and confirm the safety and clinical utility of BTVA applied unilaterally for lung volume reduction in patients with upper lobe predominate heterogeneous severe emphysema.

NCT ID: NCT01102426 Completed - Clinical trials for Relapsed/Refractory Multiple Myeloma

Aplidin - Dexamethasone in Relapsed/Refractory Myeloma

ADMYRE
Start date: June 2010
Phase: Phase 3
Study type: Interventional

Study of Plitidepsin in combination with dexamethasone versus dexamethasone alone in patients with relapsed/refractory multiple myeloma.

NCT ID: NCT01101776 Completed - Multiple Sclerosis Clinical Trials

Post Marketing Surveillance Study to Evaluate the Tolerability of Rebif® New Formulation in Patients With Relapsing Multiple Sclerosis in an Australian Clinical Setting.

ReNew
Start date: January 2010
Phase: N/A
Study type: Observational

This observational multicentric study is planned to assess the tolerability of Rebif New Formulation in an Australian clinical setting by the incidence of injection site reactions (ISRs). The study will allow the comparison of tolerability data with historical data for both Rebif New and classic formulations, and will do so by using the same pre- specified preferred terms of treatment emergent adverse events as done in historical studies. In addition, the study will analyse whether interaction(s) with a nurse impacts tolerability and the impact of Rebif New Formulation on the patient's Quality of Life.

NCT ID: NCT01101282 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Does Positive Expiratory Pressure Mask Therapy Improve Recovery From Acute Exacerbations of Chronic Obstructive Pulmonary Disease?

Start date: July 2010
Phase: N/A
Study type: Interventional

This study aims to identify whether the addition of positive expiratory pressure (PEP) mask therapy to standard medical care improves clinically important outcomes in individuals with acute exacerbations of chronic obstructive pulmonary disease. It is hypothesized that those who receive the additional PEP mask therapy will show greater improvements than those who do not.

NCT ID: NCT01100892 Completed - Diabetes Clinical Trials

Cystic Fibrosis - Insulin Deficiency, Early Action

CF-IDEA
Start date: December 2010
Phase: Phase 3
Study type: Interventional

Cystic Fibrosis (CF) is the most common life-threatening genetic condition affecting Australian children. As well as repeated lung infections, children with CF develop insulin deficiency and eventually diabetes. The CF-IDEA trial (Cystic Fibrosis - Insulin Deficiency, Early Action) will determine whether starting insulin treatment before the onset of diabetes (earlier than current practice) will improve the health of children with CF by improving body weight and lung function.

NCT ID: NCT01100411 Completed - Myopia Clinical Trials

Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate changes in contact lens geometry after lens wear

NCT ID: NCT01098903 Completed - Cancer Clinical Trials

Predictive Value of Drug Elimination Gene Polymorphisms on Clearance and Dose Adjustment of Sunitinib in Cancer Patients

CLEARSUN
Start date: January 2009
Phase: N/A
Study type: Observational

Sunitinib is an anticancer drug, but like most drugs, the effect varies from person to person. This is partly due to a variation in how well each person eradicates the drug from the body. This can lead to toxicity if the drug is eliminated slowly. Just as important is inadvertent underdosing in people who eliminate the drug quickly which may lead to a reduced anti-cancer effect. The investigators group has developed a battery of tests that may measure how an individual clears a drug from their body. The investigators intend to apply these tests to a group of patients taking sunitinib to see whether any test will help predict the level of sunitinib in the body and also the side effects. If a test seems to be promising from this study it may be possible to do a simple test on patients before they receive sunitinib so the best dose is chosen. The tests involve identifying the genes that are involved with drug elimination (CYP3A, ABCB1, ABCG2, OCT1, OATP) as well as directly measuring elimination using marker drugs (midazolam clearance and sestamibi liver clearance).

NCT ID: NCT01098539 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Study of the Efficacy and Safety of Albiglutide in Subjects With Type 2 Diabetes With Renal Impairment.

Start date: May 2010
Phase: Phase 3
Study type: Interventional

This randomized, double-blind, active-controlled study evaluates the efficacy and safety of a weekly dose of albiglutide as compared with sitagliptin. Subjects who are renally impaired with a historical diagnosis of type 2 diabetes mellitus and whose glycemia is inadequately controlled on their current regimen of diet and exercise or their antidiabetic therapy of metformin, thiazolidinedione, sulfonylurea, or any combination of these oral antidiabetic medications will be recruited into the study.

NCT ID: NCT01094769 Completed - Clinical trials for Diabetic Nephropathies

Sympathetic Nervous System Inhibition for the Treatment of Diabetic Kidney Disease

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether moxonidine is effective in reducing urine albumin levels in patients with diabetic kidney disease.