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Syndrome clinical trials

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NCT ID: NCT00673608 Completed - Clinical trials for Myelodysplastic Syndromes

Magnetic Resonance Imaging (MRI) Assessments of the Heart and Liver Iron Load in Patients With Transfusion Induced Iron Overload

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

This study will evaluate the change in cardiac iron load over a 53 week period measured by MRI in 2 cohorts of patients

NCT ID: NCT00672087 Completed - Clinical trials for Painful Bladder Syndrome

Diagnostic Challenges in IC (and Male CPPS)

Start date: September 2003
Phase:
Study type: Observational

The etiology and pathogenesis of interstitial cystitis (IC) and its related condition in men, chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) has remained elusive. This has hampered development of mechanistic treatment strategies for these common, chronic and distressing medical conditions. We believe that IC and perhaps CP/CPPS are a spectrum of complex but inter-related genetic and acquired diseases resulting from the interaction of several genes regulating immune/inflammatory and neurogenic parameters and environmental factors/circumstances or exposure, culminating in the combination of pain, frequency, urgency and sexual specific symptoms. New research has delineated the dynamic and powerful association of the immune and neurogenic system in pain activation. An immune-modulated neurogenic model of IC illuminating the action of immune derived substances and pain related substances might be important in discovering the determinants of pain, voiding dysfunction and gender specific sexual problems. This inter-related dynamic model of IC disease pathogenesis could be explored for potential avenues leading to novel diagnostic and treatment strategies. We plan to identify and evaluate the sensitivity and specificity of several novel nerve and inflammation related markers in the diagnosis and follow up of IC (and CP/CPPS). By correlating the levels of urine immune and pain related substances to disease mechanisms, severity and progression, we may be able to create a human disease specific model for diagnosis and treatment.

NCT ID: NCT00671697 Completed - Clinical trials for Myelodysplastic Syndromes and Leukemia, Myeloid, Acute

Decitabine, Arsenic Trioxide and Ascorbic Acid for Myelodysplastic Syndromes and Acute Myeloid Leukemia

Start date: May 2008
Phase: Phase 1
Study type: Interventional

This study is designed to test the combination of decitabine, arsenic trioxide and ascorbic acid in patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia

NCT ID: NCT00671515 Completed - Clinical trials for Depressive Disorder, Major

Pioglitazone for the Treatment of Major Depressive Disorder Comorbid With Metabolic Syndrome

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

The goal of this study is to begin to test whether or not pioglitazone, an FDA approved medication used to treat high blood sugar, may be safe and effective in treating Major Depressive Disorder (MDD) in patients with comorbid Metabolic Syndrome (METSYN).

NCT ID: NCT00670800 Completed - Clinical trials for Polycystic Ovary Syndrome

Study of Brain Function in Women With Insulin Resistant Polycystic Ovary Syndrome

Start date: January 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of insulin resistance on brain function in women with Polycystic Ovary Syndrome (PCOS). PCOS affected women will be evaluated prior to and following 4-month treatment with Metformin. Additionally, brain function in women with PCOS will be compared to the brain activity in normal control subjects with regular menstrual cycles.

NCT ID: NCT00669695 Terminated - Clinical trials for Obstructive Sleep Apnea Syndrome

Systemic Inflammation and Obstructive Sleep Apnea Syndrome: Effect of Atorvastatin

StatinflaSAS
Start date: May 2008
Phase: Phase 2
Study type: Interventional

The aim of this clinical trial is to evaluate the effect of Atorvastatin on the endothelial function improvement during the obstructive sleep apnea syndrome (OSAS) after 3 months of treatment, by a double-blind, randomized, placebo-controlled, multi-center study. An interim analysis will be performed when 25 patients per group will be included.

NCT ID: NCT00669266 Recruiting - Pheochromocytoma Clinical Trials

Adrenal Tumors - Pathogenesis and Therapy

Start date: September 2002
Phase:
Study type: Observational

The pathogenesis of adrenal tumors is still not fully elucidated and the treatment options for malignant tumors are poor. The current study investigates different aspects of the pathogenesis of adrenal tumors and evaluates different therapeutic options in patients with adrenocortical carcinoma.

NCT ID: NCT00668980 Completed - Down Syndrome Clinical Trials

Symbolic Representation in Young Children With Down Syndrome

Start date: July 2006
Phase: N/A
Study type: Observational

The aim of this study is to characterize the process of constitution of symbolic representation in infants with Down syndrome, as well as to investigate the relationship between gestures and the emergence of oral language. The investigators hypothesis is that children with Down syndrome could present difficulties during the constitution of symbolic representation that may be related to later deficits on expressive language, generally observed in these children.

NCT ID: NCT00668564 Terminated - Clinical trials for Niemann-Pick Disease, Type C

Hematopoietic Stem Cell Transplantation (HCT) for Inborn Errors of Metabolism

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

The primary objective of this clinical trial is to evaluate the ability to achieve and sustain donor engraftment in patients with lysosomal and peroxisomal inborn errors of metabolism undergoing hematopoietic stem cell transplantation (HCT).

NCT ID: NCT00666887 Completed - Clinical trials for Early Single Relapse of Multiple Sclerosis

Minocycline in Clinically Isolated Syndromes (CIS)

MinoCIS
Start date: January 2009
Phase: Phase 3
Study type: Interventional

The aim of the trial is to demonstrate that 100 mg of oral minocycline twice daily reduces the conversion of CIS to McDonald Criteria MS (McDMS) by an absolute 25% as compared to placebo, over a 6 month follow-up period (primary outcome). A key secondary outcome is to confirm that this early treatment benefit is maintained at two years.