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NCT ID: NCT01007474 Withdrawn - Bradycardia Clinical Trials

One Hospital ClinicalService Project

OHCS
Start date: January 2004
Phase:
Study type: Observational

The One Hospital ClinicalService Project is an integrated system composed by a network of International Hospital Departments, a clinical data repository and a shared environment for the collection, management, analysis and reporting of clinical and diagnostics data from patients treated by Medtronic therapies or patients wearing Medtronic implantable devices used within their intended use. The One Hospital ClinicalService is composed by a suite of systematic, data-guided activities designed to bring about immediate improvements in health delivery in particular settings. Data are prospectively collected. An independent committee of physicians prospectively identifies key clinical questions on a yearly basis for development of quality improvement activities, analyses and publications. A charter, approved by Hospital Istitutional Review Boards or other Hospital entities, assigns the ownership of data to the centers and governs the conduct of the project and the relationship of the scientific committee and Medtronic. Hospital is the data controller, while Medtronic is the data processor on behalf of the Hospital. Data collected for quality improvement purposes may be mined to perform clinical research.

NCT ID: NCT01002209 Withdrawn - Diabetes Clinical Trials

Postoperative Hyperbaric Oxygen Treatments to Reduce Complications in Diabetic Patients Undergoing Vascular Surgery

HODiVA
Start date: October 2019
Phase: Phase 2/Phase 3
Study type: Interventional

This trial aims to evaluate if hyperbaric oxygen treatment (HBO) given postoperatively is effective in reducing healing time and wound complications after lower extremity bypass surgery in patients with diabetes. Hypothesis: Postoperative HBO treatment is effective in reducing complications in patients with diabetes undergoing peripheral vascular surgery

NCT ID: NCT00837655 Withdrawn - Insulin Resistance Clinical Trials

Effect of Sevelamer on Glucose Tolerance and Insulin Sensitivity in Patients With Chronic Renal Failure (CKD)

SIR
Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to perform a randomized, controlled clinical trial to investigate if the phosphate binder sevelamer can improve insulin resistance and glucose handling in patients receiving maintenance hemodialysis.

NCT ID: NCT00825604 Withdrawn - Clinical trials for Stable Angina Pectoris

Quality of Life and Target Achievement After Treatment of Patients With Stable Angina Pectoris

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

The purpose of this study is to, in patients with stable angina pectoris, assess the additional benefit of PCI on top of optimized medical treatment, physical training and smoking cessation with regard to quality of life, achievement of target of treatment and clinical events such as death, acute myocardial infarction, stroke and revascularization.

NCT ID: NCT00814112 Withdrawn - Septic Shock Clinical Trials

Glycosaminoglycans During Septic Shock - a Temporal Study

GAGS
Start date: November 2008
Phase:
Study type: Observational

We have previously shown that the plasma level of glycosaminoglycans (GAG) in septic shock patients are elevated compared to controls. The purpose of this study is to investigate the temporal dynamic of the blood level of GAG in ten septic shock patients. In addition, to assess the kinetics of GAG during septic shock we examine the liver function by galactose elimination capacity as well as excreted urinary GAG.

NCT ID: NCT00700362 Withdrawn - Diabetes Mellitus Clinical Trials

Insulin Infusion and Infectious Diabetic Foot Ulcers (IIIFU)

Start date: December 2011
Phase:
Study type: Observational

Normoglycemia is important for the outcome of surgical and medical conditions. Insulin infusions have been studied to achieve normoglycemia during these circumstances and have proved to be useful. Insulin given by subcutaneous injections has longer duration compared to intravenous given insulin which makes it more difficult to control. The hypothesis behind the trial is the concept that insulin infusion is more effective in reaching normoglycemia in diabetic subjects during foot ulcer infection and surgical wound infection. - The study evaluates a target controlled insulin infusion or conventional therapy as antidiabetic treatment during foot ulcer infection and surgical wound infection. - Secondary efficacy parameter will be hospital stay, laboratories for inflammation and oxidative stress.

NCT ID: NCT00487851 Withdrawn - Clinical trials for Pancreatic Neoplasms

Comparing Endoscopic Based Stent Strategy Versus Bypass Surgery in Non-resectable Periampullary Cancer

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

Randomized study comparing endoscopic stent insertion strategy versus double-bypass surgery in non-resectable periampullary cancer

NCT ID: NCT00390026 Withdrawn - Clinical trials for Age-related Macular Degeneration

The Avastin vs Visudyne for Neovascular AMD Study

Start date: November 2006
Phase: Phase 3
Study type: Interventional

The object of the study is to compare the treatment effect of bevacizumab (Avastin), an antibody targeting vascular endothelial growth factor, with verteporfin photodynamic therapy (PDT) for patients with neovascular age-related macular degeneration, the leading cause of vision severe loss in the Western world.

NCT ID: NCT00313976 Withdrawn - Multiple Sclerosis Clinical Trials

Study to Compare Double-dose Betaferon to the Approved Dose, for Patients With Early Secondary Progressive Multiple Sclerosis (SPMS)

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate if the higher dose can give greater efficacy without negative impact on the adverse event profile for patients with early secondary progressive Multiple Sclerosis (SPMS).

NCT ID: NCT00216931 Withdrawn - Clinical trials for Respiratory Distress Syndrome

Treatment of Elevated Arterial Pulmonary Pressure With Inhaled Iloprost

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

The purpose of this study is to determine if iloprost is effective in the treatment of elevated arterial pulmonary pressure in children with ventilator treated respiratory distress syndrome.