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Syndrome clinical trials

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NCT ID: NCT00914940 Terminated - Leukemia Clinical Trials

Selective Depletion of CD45RA+T Cells From Allogeneic Peripheral Blood Stem Cell Grafts for the Prevention of GVHD

Start date: December 17, 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Allogeneic hematopoietic stem cell transplant (HSCT) is a treatment that can cure acute leukemia and myelodysplasia. After giving the patient chemotherapy and total body irradiation to stop the growth of cancer and remove the patient's diseased bone marrow, healthy stem cells from a donor are infused into the patient to replace the patient's bone marrow and make red and white blood cells and platelets. Unfortunately HSCT is often complicated by 'graft versus host disease' (GVHD) in which the transplanted cells from a donor can make an immune response against the body's normal cells and cause tissue damage and severe symptoms. Removing a subset of the donor T cells, called 'naive T cells', before transplant may reduce the frequency and intensity of GVHD. PURPOSE: This phase II trial will determine whether the removal of the naive T cells from donor cells can decrease the rate and severity of graft-vs-host disease while preserving specific immunity against infections in patients with acute leukemia or advanced myelodysplastic syndromes.

NCT ID: NCT00914823 Recruiting - PCOS Clinical Trials

Kisspeptin Administration in the Adult

Start date: June 23, 2009
Phase: Phase 1
Study type: Interventional

The goal of this study is to learn about the role of kisspeptin in the reproductive system. Kisspeptin is a naturally occurring hormone in humans that causes the release of other hormones, including gonadotropin-releasing hormone (GnRH) in the body.

NCT ID: NCT00914251 Recruiting - Metabolic Syndrome Clinical Trials

Vascular Effects of Hesperidin in Metabolic Syndrome

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

It has been suggested that cardiovascular risk factors either independently or in cluster (metabolic syndrome) increase the risk of both type 2 diabetes (DM2) and cardiovascular diseases (CVD). Consumption of citrus fruits is linked to reduced cardiovascular morbidity and mortality. Hesperidin is a flavanone abundant in citrus fruit with putative vasodilator actions in vitro. While molecular mechanisms of vascular actions of hesperidin begin to be explored, no data on in vivo vascular effect of this flavanone has been ever acquired.

NCT ID: NCT00912925 Completed - Clinical trials for Mucopolysaccharidosis I

Clinical Study of Aldurazyme in Patients With Mucopolysaccharidosis (MPS) I

Start date: December 2000
Phase: Phase 3
Study type: Interventional

This study is being conducted to demonstrate the safety and clinical efficacy of Aldurazyme treatment in MPS I patients

NCT ID: NCT00912171 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Efficacy of Oral Leukotriene in Long Term Therapy of Mild and Moderate Obstructive Sleep Apnea Syndrome in Children

SB-OSAS
Start date: January 2009
Phase: Phase 4
Study type: Interventional

The aim of the project is to evaluate whether therapy with leukotriene may be a valid therapeutic approach in children with adenotonsillar hypertrophy and with mild and moderate obstructive sleep apnea syndrome (OSAS) and to evaluate whether leukotriene is less, equally or more efficient than nasal steroid.

NCT ID: NCT00911885 Completed - Metabolic Syndrome Clinical Trials

A Simple Dietary Message to Improve Dietary Quality for Metabolic Syndrome

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

Identifying a simple dietary recommendation for weight loss and metabolic health may demonstrate potential for a simple public health message to impact coronary heart disease (CHD) prevention and metabolic syndrome. In a randomized clinical trial, the investigators propose to compare the efficacy of two intervention approaches to dietary change for CHD prevention among persons with metabolic syndrome. The two approaches are 1) the AHA Dietary Guidelines; and 2) a simple dietary change condition that focuses on increasing fiber. The investigators hypothesize that a message promoting high fiber intake may be the simple message that has potential to produce broad impact.

NCT ID: NCT00911612 Completed - Clinical trials for Irritable Bowel Syndrome

Does Welchol (Colesevelam Hydrochloride) Improve Colonic Transit in Diarrhea-predominant Irritable Bowel Syndrome (D-IBS)?

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

Our hypothesis is that the medication approved for treatment of high blood cholesterol levels, Colesevelam HCl (WELCHOL), decreases colonic transit and permeability in patients with diarrhea due to irritable bowel syndrome. This effect is thought to result from the effect of the medication on bile acids, which can cause diarrhea.

NCT ID: NCT00911313 Completed - Clinical trials for Polycystic Ovary Syndrome

Letrozole or Combined Metformin Clomiphene Citrate (CC) for Women With CC Resistant Polycystic Ovary Syndrome

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

The purpose of this study is to compare and determine the efficacy of letrozole administration to that of combined metformin and Clomiphene in infertile women with polycystic ovary syndrome (PCOS) not responding to treatment with Clomiphene alone.

NCT ID: NCT00911066 Completed - Clinical trials for Acute Lymphoblastic Leukemia

MLN4924 for the Treatment of Acute Myelogenous Leukemia, Myelodysplastic Syndrome, and Acute Lymphoblastic Leukemia

Start date: June 2009
Phase: Phase 1
Study type: Interventional

An open-label, multicenter, phase 1, dose escalation study of MLN4924 in adult patients with acute myelogenous leukemia (AML), high-grade myelodysplastic syndrome (MDS). The patient population will consist of adults previously diagnosed with AML including high-grade MDS for which standard curative, life-prolonging treatment does not exist or is no longer effective.

NCT ID: NCT00910858 Completed - Clinical trials for Low- or Intermediate-1-risk Myelodysplastic Syndrome (MDS)

A Pharmacokinetic And Pharmacodynamic Study Of Oral Lenalidomide (Revlimid) In Subjects With Low- Or Intermediate-1-Risk Myelodysplastic Syndromes

Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess pharmacokinetic and pharmacodynamic characteristics of oral lenalidomide monotherapy administered to patients with Low- or Intermediate-1-risk Myelodysplastic Syndrome (MDS).