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Syndrome clinical trials

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NCT ID: NCT00486551 Completed - ADHD Clinical Trials

Anger Control Training for Youth With Tourette Syndrome

Start date: August 2001
Phase: N/A
Study type: Interventional

This is a clinical study of a cognitive-behavioral therapy known as anger control training in adolescents with Tourette Syndrome and explosive, disruptive behavior. ACT is compared to treatment as usual (TAU) in a randomized clinical trial.

NCT ID: NCT00485368 Completed - Marfan Syndrome Clinical Trials

Angiotensin Converting Enzyme Inhibitors in Marfan Syndrome

Start date: January 2004
Phase: Phase 3
Study type: Interventional

The purpose of this research is to assess the effects of a drug called perindopril on the aorta in people known to have Marfan Syndrome. The aorta is the major artery of the body that comes out of the heart and supplies blood to the body. We know that in people with Marfan Syndrome, the aorta is stiff and this stiffness results in its enlargement over many years. This enlargement of the aorta can be very serious. We know from treatment of other heart conditions that drugs of the same type as perindopril reduce stiffness of the arteries. This type of drug has never been tried in people with Marfan Syndrome.

NCT ID: NCT00485121 Completed - Obesity Clinical Trials

Effects of Ezetimibe Add-On to Statin Therapy on Adipokine Production in Obese and Metabolic Syndrome Patients With Atherosclerosis

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

The purpose of this study is to investigate the effects of adding ezetimibe to statin therapy on levels of inflammatory markers and adipokines in patients with atherosclerosis disease and features of the metabolic syndrome,whose LDL-c remains above target (> 2.0 mmol/L) despite statin monotherapy. We hypothesize that the addition of Ezetimibe (10mg per day for 12 weeks) to ongoing statin therapy in patients with atherosclerosis and features of the metabolic syndrome will favourably modify levels of inflammatory biomarkers and adipokines.

NCT ID: NCT00484705 Completed - Clinical trials for Polycystic Ovary Syndrome

Polycystic Ovary Syndrome (PCOS) - Effect Of Physical Exercise And Electroacupuncture

PCOSNTS
Start date: October 2005
Phase: N/A
Study type: Interventional

Hypothesis: The overall hypothesis is that women with PCOS, both obese and non-obese, have larger adipocytes, altered metabolism and signs of inflammation in adipose tissue and that these changes are associated with high sympathetic nerve activity, hyperandrogenism hyperinsulinaemia, insulin resistance with progression to type II diabetes and cardiovascular disease (CVD) as well as psychological distress and reduced quality of life. Physical exercise and electro-acupuncture decrease high concentrations of androgens, induce regulare menstrual pattern, inhibits high sympathetic activity and restore the PCOS induced disturbances.

NCT ID: NCT00482859 Completed - Clinical trials for Fibromyalgia Syndrome

Sleep Disturbance and Sleep Quality in Women With Fibromyalgia Syndrome

Start date: April 2007
Phase: N/A
Study type: Observational

The purpose of this week long study is to describe sleep and problems with sleep in women diagnosed with Fibromyalgia syndrome.

NCT ID: NCT00482794 Recruiting - Clinical trials for Antiphospholipid Syndrome

Genetic Risk Factors Associated With Antiphospholipid Antibody Syndrome

APS
Start date: June 2006
Phase:
Study type: Observational

Antiphospholipid antibody syndrome (APS) is characterized by the presence of antiphospholipid antibodies, which are proteins in the blood that interfere with the body's ability to perform normal blood clotting. Clinical problems associated with antiphospholipid antibodies include an increased risk for the formation of blood clots in the lungs or deep veins of the legs, stroke, heart attack, and recurrent miscarriages. It is possible that some people with APS have a genetic predisposition for developing the syndrome. This study will use a genetic strategy to identify potential inherited risk factors for the development of APS by recruiting people with APS who have family members also affected by the syndrome or by another autoimmune disorder, such as lupus or rheumatoid arthritis.

NCT ID: NCT00481143 Completed - Clinical trials for Myelodysplastic Syndromes

Efficacy and Safety of Deferasirox in Patients With Myelodysplastic Syndrome and Transfusion-dependent Iron Overload

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

The purpose of this study is to investigate the effects of iron chelation using deferasirox in low and INT-1 risk (referring to the international prognostic scoring system, IPSS) MDS patients who show signs of iron overload due to repeated blood transfusions. This trial is not recruiting patients in the United States.

NCT ID: NCT00481130 Recruiting - Alport Syndrome Clinical Trials

Alport Syndrome Treatments and Outcomes Registry

ASTOR
Start date: September 2007
Phase:
Study type: Observational [Patient Registry]

ASTOR's primary purpose is to enroll families and patients with a history of Alport syndrome in a central registry. The information we gather will be used as a basis for studies designed to test potential treatments for Alport syndrome. ASTOR also aims to provide patients, families and physicians with the most up-to-date information about Alport syndrome.

NCT ID: NCT00480987 Terminated - Leukemia Clinical Trials

Oxaliplatin, Fludarabine, and Cytarabine in Acute Myeloid Leukemia (AML) or High-Risk Myelodysplastic Syndromes (MDS)

Start date: July 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this clinical research study is to find the highest tolerable dose of oxaliplatin combined with fludarabine plus cytarabine that can be given to patients with Acute Myeloid Leukemia (AML) or High-Risk Myelodysplastic Syndromes (MDS). Once the highest tolerable dose of oxaliplatin in this drug combination is found, the next goal of the study will be to learn the safety and the ability of the drug combination to control the disease.

NCT ID: NCT00480337 Completed - Clinical trials for Polycystic Ovary Syndrome

In Vitro Maturation of Immature Oocytes

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of this study is to aspirate immature oocytes from antral follicles and mature the oocytes in vitro. These mature oocytes will serve for fertilization and the creation of embryos which will be replace in the uterus as performed during normal IVF.We will record the efficacy and safety of this procedure.