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NCT ID: NCT00160108 Completed - Obesity Clinical Trials

A Dietary Intervention- Randomized Controlled Trial (DIRECT) Study; BGU-Harvard-Robarts Collaboration

Start date: July 2005
Phase: Phase 1
Study type: Interventional

Aim-to conduct a randomized clinical intervention study to compare three diets (low-fat, low-carbohydrate and Mediterranean diet) for weight loss

NCT ID: NCT00159887 Completed - Clinical trials for Pulmonary Hypertension

Study to Assess the Longterm Safety of Sildenafil Citrate in Patients With Pulmonary Arterial Hypertension

Start date: December 2002
Phase: Phase 3
Study type: Interventional

Open label extension study to the pivotal efficacy study to assess the safety of sildenafil citrate in patients with pulmonary arterial hypertension

NCT ID: NCT00159861 Completed - Clinical trials for Pulmonary Hypertension

The Efficacy and Safety of Sildenafil Citrate Used in Combination With Intravenous Epoprostenol in PAH

Start date: July 2003
Phase: Phase 3
Study type: Interventional

Determination of the effects of sildenafil citrate and epoprostenol when used in combination in patients with pulmonary arterial hypertension

NCT ID: NCT00159068 Completed - HIV Infection Clinical Trials

Analysis of Genetic Factors Which May Influence the Course of HIV Infection

Start date: February 2004
Phase: N/A
Study type: Observational

Patients with HIV an have a variable course of their infection. We are trying to identify factors which worsen or ameliorate the course of the disease. Such factors may be related to metabolism (breakdown) of drugs or to iron handling by the body.

NCT ID: NCT00159055 Withdrawn - CMV Disease Clinical Trials

Adoptive Immunotherapy for CMV Disease

Start date: February 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Treatment strategy of patients: Stem cell engraftment (myeloablative or NST) for induction of host vs graft myeloablative transplantation tolerance. Whenever indicated, additional post NST DLI given in graded increment, to optimize control of GVHD. Preparation of immune donor lymphocytes, either by donor immunization in-vitro with a CMV-specific peptide followed by administration of immunized donor lymphocytes, or by injection of donor lymphocytes and in-vivo sensitization of donor lymphocytes in the patient following DLI. Pre-emptive treatment of seronegative patients at risk or patients with documented viremia or CMV disease with CMV-specific donor lymphocytes generated in-vivo in the donor or in the host by peptide immunization. Consenting donors will be immunized with CMV-specific peptides, for induction of CTLs in-vivo following subcutaneous inoculation of peptides with adjuvant or donor APC pulsed with relevant peptides.

NCT ID: NCT00159042 Completed - Beta Thalassemia Clinical Trials

Genetic Factors Affecting the Severity of Beta Thalassemia

Start date: July 2004
Phase: N/A
Study type: Observational

Patients with genetic diseases can have widely differing severities. We are looking for genetic factors which influence the severity of beta thalassemia.

NCT ID: NCT00159029 Completed - Alpha Thalassemia Clinical Trials

Genetics of Alpha Thalassemia in Israeli Ethnic Groups

Start date: April 1, 2004
Phase: N/A
Study type: Observational

Alpha thalassemia causes mild anemia and is found in many ethnic groups. Usually it is found in regions where malaria is endemic. We have found that alpha thalassemia is common in Ashkenazim, whose countries of origin are in temperate climates. We are analyzing the alpha globin genes of individuals of many ethnic groups and will compare to try to define the origin of thalassemia in these individuals of European extraction.

NCT ID: NCT00159016 Withdrawn - Clinical trials for Metastatic Solid Tumors.

Role of Glivec in Patients With Tumor Cells Positive for C-kit or PDGFR; a Multi Center Study.

Start date: August 2002
Phase: Phase 2
Study type: Interventional

This is a phase II, multi-center (Israeli), open label, non-randomized trial for every patient with the specified tumors expressing c-kit or PDGFR. Expression of these kinases will be investigated in tumor samples obtained at the time of diagnosis or from the time of recurrent disease. Every patient with positive expression of either of the kinases will be evaluated for quantitative and qualitative evidence of disease prior to entry into the study, and if possible, no other treatment will be given concomitantly, to allow evaluation of the net effect of Glivec on tumor growth kinetics, searching for measurable evidence of response. Glivec is supplied to the study investigators by Novartis Pharmaceutical. Patients will receive Glivec 400mg-800mg p.o./day for an exposure period of up to 12 months provided that in the opinion of the investigator the patient is benefiting from treatment with Glivec, and in the absence of any safety concern. For patients with brain tumors who are not receiving concomitant enzyme inducing anti-convulsant drugs, the recommended dose of Glivec is 800mg/day.

NCT ID: NCT00159003 Completed - Clinical trials for Acute Myeloid Leukemia

Analysis of Genetic Factors Related to Predisposition and Prognosis of Hematological Malignancies in Israel

Start date: January 1, 1998
Phase: N/A
Study type: Observational

There are naturally occuring variations in the genetic makeup of all of us. Some of these variations may contribute to a change in susceptibility toward different diseases or change the prognosis. We are studying these genetic variations in patients with leukemia. The genes we are studying are those which influence detoxification of drugs and toxins.

NCT ID: NCT00158990 Completed - Bipolar Disorder Clinical Trials

Triiodothyronine (T3) Supplementation in the Treatment of Bipolar and Unipolar Depression.

Start date: October 2002
Phase: Phase 3
Study type: Interventional

The purpose of this project is to determine whether concurrent treatment of patients with major depression (unipolar or bipolar) with triiodothyronine (T3) and sertraline, will lead to a stronger and/or more rapid antidepressant effect than treatment with sertraline alone.