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NCT ID: NCT00315965 Recruiting - Clinical trials for Pulmonary Diffusing Capacity

Development of a New Method for Steady-State Measurement of NO Lung Diffusing Capacity in Healthy Subjects

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

Using a rapidly responding nitric oxide analyzer in a new developed modular lung-function-setup we are going to measure steady-state NO diffusing capacity in 107 healthy subjects (age 6-45 years). The results will be compared to those measured by using carbon monoxide single-breath estimates. We like to show that the new method is sufficient to measure exactly lung diffusion capacity in this collective.

NCT ID: NCT00311857 Recruiting - Clinical trials for Glioblastoma Multiforme

Safety Study of Cetuximab, Radiotherapy and Temozolomide in Primary Glioblastoma Multiforme(GERT)

Start date: February 2006
Phase: Phase 1/Phase 2
Study type: Interventional

GERT is a one-armed single-center phase I/II trial. In a first step, dose-escalation of TMZ from 50 mg/m2 to 75mg/m2 together with radiotherapy and cetuximab will be performed. Should safety be proven, the phase II trial will be initiated with the standard dose of 75mg/m2 of TMZ. Cetuximab will be applied in the standard application dose of 400mg/m2 in week 1, thereafter at a dose of 250mg/m2 weekly. A total of 46 patients will be included into this phase I/II trial. Primary endpoints are feasibility and toxicity, secondary endpoints are overall and progression-free survival. An interim analysis will be performed after inclusion of 15 patients into the main study. Patients’ enrolment will be performed over a period of 2 years. The observation time will end 2 years after inclusion of the last patient.

NCT ID: NCT00311337 Recruiting - Multiple Myeloma Clinical Trials

VELCADE as Maintenance Treatment in Patients With Multiple Myeloma Following Autologous Peripheral Blood Stem Cell Transplantation (PBSCT)

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

Protocol DSMM VIII is a multi-center, open-label study evaluating the safety and tolerability, as well as the efficacy, of maintenance treatment with VELCADE (bortezomib) in patients with multiple myeloma with detectable disease activity following tandem high-dose chemotherapy and autologous SCT. The time from SCT to the initiation of VELCADE treatment will be 3 to 6 months.

NCT ID: NCT00310583 Recruiting - Neuropathic Pain Clinical Trials

Effects of Pregabalin on Mechanical Hyperalgesia

Start date: July 2006
Phase: Phase 4
Study type: Interventional

The aim of this randomized placebo-controlled study is to evaluate the effects of analgetics for neuropathic pain on mechanical hyperalgesia as a kind of evoked pain. Therefore the number of responders and non-responders on pregabalin will be evaluated in respect of mechanical hyperalgesia (stimulus-response-function (SRF) on static punctual stimuli evoking pain determined via pinprick). The hypothesis is that in the placebo group the amount of non-responders is increased.

NCT ID: NCT00309920 Recruiting - Breast Cancer Clinical Trials

Combination Chemotherapy With or Without Darbepoetin Alfa in Treating Women With Stage III Breast Cancer

Start date: January 2004
Phase: N/A
Study type: Interventional

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Colony-stimulating factors, such as darbepoetin alfa, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Giving combination chemotherapy together with darbepoetin alfa after surgery may kill any tumor cells that remain after surgery. It is not yet known whether combination chemotherapy and darbepoetin alfa are more effective than combination chemotherapy alone in treating stage III breast cancer. PURPOSE: This randomized clinical trial is studying how well giving combination chemotherapy together with darbepoetin alfa works compared to combination chemotherapy alone in treating women with stage III breast cancer.

NCT ID: NCT00306124 Recruiting - Healthy Clinical Trials

Dopaminergic Enhancement of Learning and Memory in Healthy Adults and Patients With Dementia/Mild Cognitive Impairment

Start date: January 2006
Phase: Phase 4
Study type: Interventional

This study aims to determine whether levodopa is effective in boosting learning and memory in healthy subjects and patients with dementia or Mild Cognitive Impairment. We also examine in healthy subjects using functional magnetic resonance imaging which brain regions mediate improved learning after levodopa administration.

NCT ID: NCT00300651 Recruiting - Schizophrenia Clinical Trials

Trial of Cognitive Behavioral Therapy for Schizophrenia

Start date: March 2006
Phase: Phase 3
Study type: Interventional

The following study addresses the hypothesis that cognitive-behavioral interventions will be effective in reducing positive and negative symptoms of schizophrenia under the conditions of the German health care system. It is also hypothesized that interventions designed to reduce delusions will reduce cognitive biases and dysfunctional self-concepts.

NCT ID: NCT00292383 Recruiting - Clinical trials for Atrioventricular Block

Ventricular Pacing Site Selection (V-PASS)

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether there is a relationship between ventricular lead position and the incidence of heart failure and atrial fibrillation in patients with indication for permanent pacemaker stimulation.

NCT ID: NCT00292357 Recruiting - Diabetic Foot Clinical Trials

Local Application of Autologous Bone Marrow Cells for Treatment of Chronic Diabetic Ulcers

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

Bone marrow cells were previously shown to enhance wound healing in experimental diabetes. In this pilot study, patients with chronic diabetic ulcers not healing under conventional therapy, will be treated with local application of autologous bone marrow cells.

NCT ID: NCT00291460 Recruiting - COPD Clinical Trials

Inspiratory Muscle Training in Hypercapnic COPD

Start date: February 2006
Phase: Phase 4
Study type: Interventional

The trial intends to investigate, whether inspiratory muscle training in hypercapnic patients improves inspiratory muscle strength, inspiratory muscle endurance and endurance to walk within six minutes.