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NCT ID: NCT00890825 Completed - Clinical trials for Non Small Cell Lung Cancer

AZD6244 in Combination With Docetaxel Versus Docetaxel Alone in KRAS Mutation Positive NSCLC Patients

Start date: April 20, 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the efficacy of AZD6244 in combination with docetaxel versus docetaxel alone in patients with KRAS mutation positive locally advanced or metastatic non small cell lung cancer.

NCT ID: NCT00890214 Completed - Clinical trials for Acute Kidney Failure

Prostacyclin's Effect on Platelet Responsiveness

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

The researchers investigated the influence of a prostacyclin analogue (PGIA) versus unfractionated heparin (UFH) on ex vivo platelet function, during continuous venovenous hemodiafiltration.

NCT ID: NCT00889863 Completed - Clinical trials for Systemic Juvenile Idiopathic Arthritis With Active Flare

Flare Prevention Study of Canakinumab in Patients With Active Systemic Juvenile Idiopathic Arthritis (SJIA)

ß-SPECIFIC 2
Start date: July 2009
Phase: Phase 3
Study type: Interventional

This two-part study assessed the sustained efficacy of canakinumab in the double-blind Part II and the ability to taper steroids in the open label Part I.

NCT ID: NCT00889720 Completed - Smoking Cessation Clinical Trials

A Pilot Study Of Smoking Cessation Treatment Including Varenicline In Patients Scheduled For Planned Surgery

Start date: November 2009
Phase: Phase 4
Study type: Interventional

It is possible to offer smoking cessation treatment including varenicline to patients scheduled for elective surgery. This study will evaluate whether or not this will enable some patients to quit smoking for up to 4 weeks prior to surgery and in turn, whether this may lead to reductions in post-operative complication such as wound infections.

NCT ID: NCT00889382 Completed - Ovarian Cancer Clinical Trials

A Study Evaluating Intermittent and Continuous OSI-906 and Weekly Paclitaxel in Patients With Recurrent Epithelial Ovarian Cancer (and Other Solid Tumors)

Start date: August 5, 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multi-center, randomized, open-label, phase 1/2 study of continuous weekly paclitaxel and escalating doses of intermittent or continuous OSI-906 in patients with recurrent/relapsed ovarian and other solid tumors.

NCT ID: NCT00889057 Completed - Osteosarcoma Clinical Trials

Sorafenib in Relapsed High Grade Osteosarcoma

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Aim of this exploratory phase II study is to assess the clinical activity of sorafenib as single agent, in terms of percentage of patients with high grade advanced osteosarcoma free from progression following 4 months of therapy

NCT ID: NCT00888836 Completed - Type 2 Diabetes Clinical Trials

Diet and Medical Therapy Versus Bariatric Surgery in Type 2 Diabetes

DIBASY
Start date: April 2009
Phase: N/A
Study type: Interventional

It is generally held that ß-cell function is irreversibly lost already at the time the disease manifests itself and thereafter continues to decline linearly with time. Several studies, however, have documented the possibility that ß-cell function may be restored, at least partially, in type 2 diabetes. Of major relevance to the issue of ß-cell recovery in diabetes are the following findings: - bariatric surgery in morbidly obese patients with type 2 diabetes can restore euglycaemia, the acute insulin response to glucose and insulin sensitivity; - recent studies have reported that diabetic subjects return to euglycaemia and normal insulin levels within days after surgery, long before a significant weight loss has occurred; and - whereas gastric bypass (GBP) improves insulin sensitivity in proportion to weight loss, bilio-pancreatic diversion (BPD) improves insulin action out of proportion to weight loss, i.e., it normalizes it at a time when patients are still markedly obese. Because RYGB is a predominantly restrictive procedure involving the foregut, whereas BPD is a predominantly malabsorptive procedure involving the distal gastro-intestinal (GI) tract, these findings suggest that the control of both insulin action and ß-cell function is influenced by signals originating from the GI tract. The principal aim of this study is to verify the effect on type 2 diabetes mellitus (T2DM) of GBP and BPD, the two operations which have shown specific actions on glucose homeostasis control, in type 2 diabetic patients with BMI > 35 kg/m2, and to compare this effect with matched T2DM control patients receiving the standard of medical care.

NCT ID: NCT00887978 Completed - Clinical trials for Pulmonary Hypertension

Efficacy and Safety of Oral UT-15C Tablets to Treat Pulmonary Arterial Hypertension

FREEDOM-C2
Start date: June 2009
Phase: Phase 3
Study type: Interventional

This study is an international, multi-center, randomized, double-blind, placebo-controlled study in subjects with PAH who are currently receiving approved therapy for their PAH (i.e., endothelin receptor antagonist and/or phosphodiesterase-5 inhibitor). Study visits will occur at 4 week intervals for 16 weeks with the key measure of efficacy being the 6-minute walk test. Study procedures include routine blood tests, medical history, physical exams, disease evaluation, and exercise tests. Patients who complete all assessments for 16-weeks will also be eligible to enter an open-label, extension phase study (FREEDOM - EXT).

NCT ID: NCT00887588 Completed - Clinical trials for Chronic Heart Failure

LCZ696 Compared to Valsartan in Patients With Chronic Heart Failure and Preserved Left-ventricular Ejection Fraction

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

The study will assess the effects of 36 weeks of treatment with LCZ696 compared to valsartan on N-terminal pro-Brain Natriuretic Peptide (NT-proBNP) in patients with chronic heart failure and preserved left-ventricular ejection fraction.

NCT ID: NCT00887354 Completed - Osteoporosis Clinical Trials

A Study That Will Compare the Effect of Two Drugs on Participants With Low Bone Mass and a Recent Hip Fracture

MOVE
Start date: April 2009
Phase: Phase 4
Study type: Interventional

This study will evaluate whether teriparatide is superior to the active comparator in the change from baseline of lumbar spine BMD (bone mineral density) in men and postmenopausal women with low bone mass and a recent pertrochanteric hip fracture.