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NCT ID: NCT00516776 Completed - Ulcerative Colitis Clinical Trials

The Innate Immune System and Inflammatory Bowel Disease

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

The study includes individuals with ulcerative colitis, Crohn's disease and healthy controls. The purpose of this study is to examine the innate immune system (IIS) by exposing peripheral blood monocytes to various ligands relevant for stimulation of the IIS and study the immune response. Colonic mucosal samples are examined to find gene expression patterns which may distinguish the two forms of disease from each other and from healthy controls. The hypothesis is that the innate immune system has responses unique for the disease states, and that the diseases may be differentiated by examination of gene expression patterns in mucosal biopsies.

NCT ID: NCT00514475 Completed - Clinical trials for Mantle Cell Lymphoma

Zevalin-BEAM/BEAC With Autologous Stem Cell Support as Consolidation in First Line Treatment of Mantle Cell Lymphoma

Start date: November 2005
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine if outcome for patients with mantle cell lymphoma is improved by adding radioimmunotherapy to high-dose regimen before auto-transplant in patients who are not in CR after induction therapy.

NCT ID: NCT00514241 Completed - Clinical trials for Coronary Heart Failure

Evaluate Use of Gravitational Platelet Separation System on Leg Wound Healing in Coronary Bypass Surgery

Start date: January 2006
Phase: Phase 1
Study type: Interventional

The aim of platelet rich plasma (PRP) application is to accelerate the healing cascade via application of elevated cytokine concentrations released during platelet degranulation. This is a prospective randomized study of the effect of autologous platelet concentrate application during surgical closure following a vein harvest during coronary bypass surgery. This prophylactic measure will be compared to standard surgical closure techniques with the primary outcome being the incidence of leg wound infection.

NCT ID: NCT00514059 Completed - Tetanus Clinical Trials

Immunogenicity and Safety Study of a Booster Dose (5th) of Diphteria-Tetanus-Pertussis-Polio Vaccine

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

An open clinical trial to study the immune response and safety after giving a booster dose (5th Dose) of a combination vaccine against Diphteria-Tetanus-Pertussis-Polio to healthy adolescents 15-16 Years of age. The first three doses were given during the first year of life, according to the Norwegian child immunization program. The fourth dose was given in a previous clinical trial performed in 1998 when the children were 6-7 years old. In 2006 there was a change in the child immunization program in Norway: a fourth dose of a Combination Vaccine Against Diphteria-Tetanus-Pertussis-Polio is given to children 6-7 years old. This study will give us information if there is need for an additional dose (5th dose) of a combination vaccine, containing the pertussis components, before the adolescents are leaving secondary school.

NCT ID: NCT00513942 Completed - Pregnancy Clinical Trials

Effects of Fetal Movement Counting in Third Trimester of Pregnancy

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

The aim is to test effects of using formal kick counting chart in the third trimester of pregnancy in an unselected population. The research questions are: Does Fetal Movement Counting (FMC): 1. Improve the identification of risk pregnancies/pathology? 2. Affect the women's well-being? 3. Stimulate maternal-fetal attachment antepartum?

NCT ID: NCT00510406 Completed - Clinical trials for Lower Urinary Tract Symptoms

A Study With Combination Treatment (Tamsulosin Hydrochloride and Solifenacin Succinate) in Male Patients With LUTS/BPH

SATURN
Start date: January 2007
Phase: Phase 2
Study type: Interventional

The study will examine the efficacy,safety and tolerability of combination therapy of tamsulosin and solifenacin compared to placebo and monotherapy of tamsulosin and solifenacin in the treatment of males with LUTS associated with BPH.

NCT ID: NCT00509652 Recruiting - Hemochromatosis Clinical Trials

Erythrocyte Apheresis Versus Phlebotomy in Hemochromatosis

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

Primary hemochromatosis is the most frequent hereditary condition in Scandinavia. The condition may result in serious organ damage which can be prevented by therapy, but only few patients develop such organ damage. The optimal treatment, therefore, is still a matter of discussion Prevention of organ damage has traditionally been accomplished by drawing of full blood (phlebotomy), which has to be frequently repeated during the initial phase and then continued indefinitely as a maintenance treatment. The removed amount of iron may be increased two- or threefold for each procedure by using modern equipment for selective removal of red blood cells (red cell apheresis). Possible drawbacks of this technique may be higher costs, prolonged time for each therapeutic procedure, and certain requirements to the patients. The possible advantages are the reduced number of therapeutic procedures and less strain for the patient. No larger, randomized study has been published in order to determine which method should be preferred. This study is a controlled trial in which participating patients are asked to be randomized to red cell apheresis or traditional phlebotomy. Each group will be followed by means of well-defined assessments in order to explore possible advantages and disadvantages of each method in order to establish what type of treatment should be recommended.

NCT ID: NCT00509457 Completed - Clinical trials for Carcinoma, Non-Small-Cell Lung

GV 1001 Immunotherapy in Patients With Non-small Cell Lung Cancer (NSCLC)

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

To examine the safety and efficacy of telomerase peptide vaccination ( stimulation of the immune system) in patients with NSCLC after having been treated with conventional therapy with radiotherapy and docetaxel as a radiosensitizer.

NCT ID: NCT00509119 Withdrawn - Stroke Clinical Trials

ICP Waveform Analysis in Stroke Patients

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

This is a study on how acute clinical state and final clinical outcome in patients with stroke (exclusive subarachnoid hemorrhage) relate to ICP/ABP-derived pressure waveform parameters recorded during intensive care management.

NCT ID: NCT00508209 Active, not recruiting - Multiple Myeloma Clinical Trials

Bortezomib and High-dose Melphalan at Myeloma Relapse

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

The prognosis after retreating with high-dose melphalan with stem cell support after first relapse after high-dose treatment is dependent on the time to first relapse. Bortezomib can increase chemosensitivity of e.g. melphalan. The trial aims at determining the toxicity of adding bortezomib to high-dose melphalan with stem cell support and evaluating whether the time to a second relapse can be prolonged.