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Syndrome clinical trials

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NCT ID: NCT00821119 Completed - Clinical trials for Respiratory Distress Syndrome

Trial of Non Invasive Ventilation for Respiratoy Distress Syndrome

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

The purpose of this study is to evaluate the hypothesis that nasal intermittent positive pressure(NIPP), used as a primary mode of ventilation in preterm infants with RDS, will decrease the need for conventional endotracheal ventilation when compared to nasal continuous positive airway pressure.(NCPAP)

NCT ID: NCT00819923 Unknown status - Clinical trials for Acute Coronary Syndrome

Comparison of Bio-Active-Stent to the Everolimus-Eluting Stent in Acute Coronary Syndrome

BASE-ACS
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of the trial is to compare the safety and effectiveness of bio-active-stent (BAS) and everolimus-eluting stent (EES) in patients presenting with acute coronary syndrome.

NCT ID: NCT00819897 Terminated - Clinical trials for Clinically Isolated Syndrome

Longitudinal Study in Clinically Isolated Syndrome (CIS) Patients Treated With Interferon Beta

QUALICIS
Start date: June 2008
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the role of cognitive disorders and quality of life in patients with CIS, considered as high risk to develop an MS, treated with interferon Beta. This prospective observational study will include 120 patients, all treated and evaluated annually with neurological extensive examination, ophthalmologic screening (OCT, OF, VEP, VF), auto questionnaire about fatigue (musicol, ELIF), quality of life (SEP-59), and conventional MRI.

NCT ID: NCT00819403 Completed - Metabolic Syndrome Clinical Trials

Simvastatin With or Without Ezetimibe and Atherothrombotic Biomarker Assessment

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

To determine whether the combination of ezetimibe and simvastatin improves biomarkers of atherothrombosis compared to simvastatin alone in patients with the metabolic syndrome.

NCT ID: NCT00818649 Terminated - Leukemia Clinical Trials

Bortezomib and Vorinostat in Treating Patients With High-Risk Myelodysplastic Syndrome or Acute Myeloid Leukemia

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

RATIONALE: Bortezomib and vorinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving bortezomib together with vorinostat may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving bortezomib together with vorinostat works in treating patients with high-risk myelodysplastic syndrome or acute myelogenous leukemia.

NCT ID: NCT00817128 Completed - Clinical trials for Complex Regional Pain Syndrome, Type I

Pain Exposure Physical Therapy (PEPT) Versus CBO in Patients With Complex Regional Pain Syndrome Type I (CRPS-1)

PEPTOC
Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The current Dutch CBO guideline treatment of Complex Regional Pain Syndrome Type I (CRPS-1) is very disappointing with chronification, disability and subsequent high medical costs and personal suffering. A possible better treatment is intensive function-oriented physical therapy or Pain Exposure in Physical Therapy (PEPT). However, there are no adequate studies performed that demonstrate the efficacy of PEPT and therefore PEPT is lacking in the Dutch CBO CRPS-1 guidelines. Despite a lacking scientific argumentation, the PEPT approach or Macedonian therapy, is now being adopted on a large scale among physical therapists in The Netherlands. There are two level C retrospective cohort studies demonstrating a promising and clinical relevant beneficial effect on pain and function after PEPT. In response to the growing demand for scientific argumentation among doctors and physical therapists with respect to the efficacy of PEPT, we conducted a pilot study at the UMC St Radboud Nijmegen. The results of this pilot study were very promising and therefore, we decided to design a large RCT to investigate the treatment effects and costs in CRPS patients treated with PEPT compared to CRPS patients treated with usual therapy according to the Dutch CBO guidelines.

NCT ID: NCT00816829 Terminated - Obesity Clinical Trials

Effect of Fenofibrate on Sleep Apnea Syndrome

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Objectives: to investigate for the potential effect of fenofibrate on symptoms and biological changes associated with sleep apnea syndrome.

NCT ID: NCT00816413 Withdrawn - Lymphoma Clinical Trials

Donor Stem Cell Transplant, Pentostatin, and Total-Body Irradiation in Treating Patients With Hematological Cancer

Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Giving low doses of chemotherapy and total-body irradiation before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Removing the T cells from the donor cells before transplant and giving cyclosporine and mycophenolate mofetil after transplant may stop this from happening. PURPOSE: This phase I/II trial is studying the side effects of giving a donor stem cell transplant after pentostatin and total-body irradiation and to see how well it works in treating patients with hematological cancer.

NCT ID: NCT00815932 Withdrawn - Clinical trials for Diabetic Neuropathies

The Effect of Transcranial Direct Current Stimulation (t-DCS) On the P300 Component of Event-Related Potentials in Patients With Chronic Neuropathic Pain Due To CRPS or Diabetic Neuropathy

Start date: September 2016
Phase: N/A
Study type: Interventional

This is a controlled trial designed to determine short- and long-term effects of repeated tDCS on the P300 component of event-related evoked potentials in patients with chronic neuropathic pain due to Complex regional Pain Syndrome (CRPS) or diabetic neuropathy as compared with healthy subjects.

NCT ID: NCT00815659 Completed - Metabolic Syndrome Clinical Trials

Effect of Crestor (Rosuvastatin) on Lipid Levels in Patients With Metabolic Syndrome

EFFORT
Start date: December 2008
Phase: Phase 4
Study type: Interventional

The primary objective is to evaluate the efficacy of rosuvastatin therapy on plasma lipid profile (Low Density Lipoprotein (LDL), High-Density Lipoprotein (HDL), total cholesterol, triglyceride) in patients with metabolic syndrome.