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NCT ID: NCT01071525 Unknown status - Clinical trials for Hypercholesterolemia

The Effect of Niacin Administration on Oxidative Stress in Patients With Hypercholesterolmia, as Measured by the Use of a Novel Biomarker

Start date: April 2010
Phase: Phase 3
Study type: Interventional

1. Treatment of Hypercholesterolemic patients with niacin will cause a significant decrease in oxidative stress and a decrease in the atherogenecity in blood samples of the patients. 2. A possible correlation between oxidative stress in hypercholesterolemic patients taking niacin to clinical hypercholesterolemia parameters is possible. 3. Using a novel biomarker will enable a precise detection of the change in the oxidative stress in hypercholesterolemic patients.

NCT ID: NCT01071486 Withdrawn - Clinical trials for GST Genetic Polymorphism

Busulfan Pharmacokinetic Analysis and GST Polymorphism in Adults Undergoing Hematological Stem Cell Transplantation

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

Between 100 up to 200 adults undergoing HSCT for their primary disease will be included in this pharmacokinetic/pharmacogenetic study. In the preparative protocol Busulfan (BU)will be included as indicated in a known protocol. The GST polymorphism (A1,M1,T1 and P1) will be investigated using real time PCR. A correlation between pharmacokinetic parameters and patients polymorphism will be performed using known statistical technics for comparison. The aims of this study are, to correlate the demographic data, clinical presentation, clinical outcomes of the included individuals, the BU kinetics and the GST polymorphism and to establish an outcome "map" for those who receive HSCT for their primary disease.

NCT ID: NCT01070914 Recruiting - Clinical trials for Primary Ciliary Dyskinesia

Early Detection and Characterization of Primary Ciliary Dyskinesia

Start date: June 2011
Phase: N/A
Study type: Observational

Primary Ciliary Dyskinesia (PCD) is a severe genetic disorder caused by various mutations in genes affecting ciliary motility. Various new and complementary diagnostic techniques, including measurements of nasal nitric oxide (NO), Video Microscopy (VM), Immunoflourescence (IF) and genetic analysis have recently been recognized as simpler and more accurate modalities for the diagnosis and characterization of patients with PCD compared to electron microscopy. While considered a rare disease worldwide, PCD is more prevalent among highly consanguineous populations, such as those found in Israel. We hypothesize that using modern state of the art and novel test modalities on a national scale in Israel will improve diagnosis, improve phenotypic-genotypic correlations and create a national registry for PCD.

NCT ID: NCT01070758 Completed - Clinical trials for Congenital Hyperinsulinism

Lanreotide Autogel Treatment of Patients With Congenital Hyperinsulinism of Infancy

Start date: February 2010
Phase: Phase 4
Study type: Interventional

The purpose of our study is to evaluate the efficacy and safety of Lanreotide Autogel in children with congenital hyperinsulinism already treated with Octreotide by pump. Congenital hyperinsulinism is a genetic disorder characterized by inappropriate insulin secretion resulting in persistent hypoglycemia (low blood sugars. Patients exposed to recurrent hypoglycemic episodes are at increased risk of developmental disorders, so identification and prompt management of patients are essential. Many patients are treated with the somatostatin analog Octreotide which is administered by continuous infusion using a pump (we use an insulin pump). This treatment may pose a huge burden and be stressful for patients and families as it demands intensive daily care. In an effort to simplify the daily care of our patients and improve their quality of life we will study the efficacy and safety of Lanreotide Autogel - a long-acting somatostatin analog that can be administered by injection once a month

NCT ID: NCT01070745 Withdrawn - Clinical trials for Patent Ductus Arteriosus

Second Course of Therapy for Resistant Patent Ductus Arteriosus (PDA)

Start date: June 2010
Phase: Phase 2
Study type: Interventional

Patency of the ductus arteriosus (PDA) is functionally essential for fetal circulation, however persistence of ductal patency postnatally may have significant adverse hemodynamic effects in the neonate. Medical therapy for PDA predominantly involves the administration of one of two non-steroidal anti-inflammatory drugs: indomethacin or ibuprofen. Both of these therapies have been shown to be successful in mediating ductal closure in approximately 70% of treated infants. However, the need for a second course of treatment for PDA closure remains quite common. The investigators hypothesize that, because of small differences between the two drugs, a greater percentage of infants who did not respond to a first course of therapy with indomethacin will respond to a second course with ibuprofen than to a repeat course of indomethacin. As such, the investigators aim to compare secondary therapy with a repeat course of indomethacin to secondary therapy with ibuprofen in infants whose ductus remained patent after a first course of therapy with indomethacin.

NCT ID: NCT01070602 Recruiting - Clinical trials for Intraoperative Floppy Iris Syndrome

The Effect of Anterior Corneal Incisions on Intraoperative Floppy Iris Syndrome (IFIS) Incidence and Severity in Tamsulosin Treated Cataract Patients

Start date: July 2010
Phase: N/A
Study type: Interventional

Intraoperative Floppy Iris Syndrome (IFIS) may occur during cataract surgeries in patients treated with alpha 1 blockers. IFIS related to alpha 1 blocker Tamsulosin (used for prostate hypertrophy) was reported in 50-90% of patients. IFIS during surgery make the surgery more difficult and raise complication rate. Using anterior corneal incisions was reported briefly in literature as a prophylactic means but was not studied prospectively. we believe (according to our clinical experience) that these anterior incisions do help to reduce the incidence and severity of IFIS signs and complications rate during surgeries.

NCT ID: NCT01070589 Recruiting - Obesity Clinical Trials

The Effect of Obesity on Growth Hormone Response to Anaerobic Exercise

Start date: February 2010
Phase: N/A
Study type: Observational

The aim of the present study is to asses the effect of obesity on anaerobic exercise's growth hormone (GH) response.

NCT ID: NCT01070277 Recruiting - Abdominal Pain Clinical Trials

Antiparasitic Treatment for Returning Travelers With Chronic Diarrhea

Start date: March 2012
Phase: N/A
Study type: Interventional

Study hypotheses is that Antiparasitic therapy in patients with chronic diarrhea after travel to a developing country, with a negative stool findings, will be significantly effective in eliminating diarrhea and other gastro-intestinal complaints compared to similar patients receiving placebo.

NCT ID: NCT01070108 Completed - Clinical trials for Postoperative Pain Management

Escalating Ketamine Doses and Pre-emption

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

Ketamine affects postoperative pain when administered intravenously immediately before, during or at the end of surgical procedures. We assessed the effects of multiple and escalating doses of ketamine administered many hours before surgery on postoperative pain and analgesia consumption.

NCT ID: NCT01069614 Not yet recruiting - Wounds Clinical Trials

A Skin Stretching Wound Closure System

Start date: n/a
Phase: Phase 1
Study type: Interventional

A skin stretching device has been designed to stretch tissue prior to surgery, during surgery and in order to secure wounds following surgery. The device may be used in non-invasive and invasive applications.