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NCT ID: NCT02194426 Completed - Neoplasms Clinical Trials

First-in-human Study to Investigate the Safety, Tolerability and Blood Levels of the Test Drug MP0250 in Cancer Patients

Start date: July 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This research study is looking at a new DARPin® drug candidate, called MP0250. There is evidence from preclinical studies that MP0250 may be effective in the treatment of cancer. This is the first study of MP0250 in humans and its main purpose is to test its safety and tolerability in patients with cancer. This study will also examine how the drug is changed by and removed from the body and look for indicators that the drug may be effective against cancer. This study will test several different dose levels of the study drug to determine the safety and tolerability profile of the drug.

NCT ID: NCT02194023 Completed - Dental Plaque Clinical Trials

Clinical Effects of Two New Chlorhexidine Digluconate Formulations: 0.12% and 0.03%.

Start date: September 2011
Phase: Phase 2
Study type: Interventional

In the current study we tested the hypothesis that new 0.05% Cetylpyridinium chloride (CPC) mouthrinse formulations containing 0.12% or 0.03% chlorhexidine digluconate (CHX): 1) yield similar or better clinical results regarding the inhibition of de novo plaque growth compared to those achieved with an already marketed 0.12% CHX mouthrinse (Perio-Aid Treatment without alcohol. Dentaid, Spain), 2) reduce the side effects caused by the marketed 0.12% CHX formula and 3) that these mouthrinses have no negative microbiological effects, and they control total bacterial loads.

NCT ID: NCT02193659 Completed - Overweight Clinical Trials

Changes Induced by Breakfast Cereals Enriched With Omega-3 in the Lipidic Profile

cereals
Start date: September 2013
Phase: N/A
Study type: Interventional

The inclusion of breakfast cereals enriched with omega-3 for female users of a pharmacy who had some lipidic profiles to the limit is highly conditioned by their nutritional acceptance. The main objective is to assess the effect of breakfast cereals intake with omega-3 on women lipid profile values to the limit, users of a pharmacy in Elche and in this way reduce the small dyslipidemia.

NCT ID: NCT02192996 Completed - Clinical trials for Other Preterm Infants

Probiotic Supplementation to Improve the GUT Microbiota of Very Low Birth Weight Preterm, a Pilot Study

Start date: December 2012
Phase: Phase 0
Study type: Interventional

This pilot trial is designed to investigate the benefits of the use of probiotics in GUT microbiota development and/or immunological biomarkers and how this can be related with the clinical status of very low birth weight preterms during their first weeks of life at the neonatal intensive care unit(NICU).

NCT ID: NCT02192788 Completed - Clinical trials for Oligometastatic Prostate Cancer

Phase II Study of SBRT as Treatment for Oligometastases in Prostate Cancer

Start date: August 2014
Phase: N/A
Study type: Interventional

This study aims to probe the effect of SBRT as a treatment oligometastases of prostate cancer, regardless of basal treatment received, and I know the response, biochemical control, the progression-free survival as well as their impact on quality of life. Primary Objective: Local and symptomatic oligometastases Control of prostate cancer treated by SBRT. Secondary Objectives: Analyzing biochemical progression rates, progression-free survival, chemotherapy-free survival and overall survival. Analyze toxicities and quality of life of patients before and after treatment

NCT ID: NCT02192554 Completed - Mental Disorder Clinical Trials

Safety Follow-up Study for Subjects With Agitation Associated With Dementia of the Alzheimer's Type Who Previously Participated in a Double-blind Trial of Brexpiprazole or Placebo

Start date: June 2014
Phase:
Study type: Observational

To follow-up on the safety of subjects who were previously treated in a double-blind trial of brexpiprazole.

NCT ID: NCT02191826 Completed - Clinical trials for Familial Amyloid Polyneuropathy (FAP)

Study of SOM0226 in Familial Amyloid Polyneuropathy

Start date: July 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Clinical proof of concept study to evaluate SOM0226 efficacy in TTR Amyloidosis.

NCT ID: NCT02191553 Completed - Depression Clinical Trials

Differential Effect of Four Mindfulness Exercises

Start date: September 2014
Phase: N/A
Study type: Interventional

Mindfulness can be considered as a family of complex attentional and emotional regulation strategies that promote the cultivation of well-being and emotional balance. The practice of mindfulness produces the development of a consciousness that unfolds moment to moment, open and unprejudiced in the present moment, here and now. Despite its extensive benefits, the practice of mindfulness requires a significant commitment in time and effort, which limits the potential for its dissemination. The studies to narrow the differential effects of the various exercises based on mindfulness, will further enhance their effectiveness and they can guide the practice sequence according to user needs. In this paper we will research mindfulness electroencephalographic correlates of as four different exercise programs included in mindfulness-based cognitive therapy (MBCT) and stress reduction program based on mindfulness (MBSR) as well as its effect on several psychological variables.

NCT ID: NCT02191150 Completed - Anaemia Clinical Trials

Study of Haemodialysis Patients Switching From Aranesp to Biosimilar

SHADE
Start date: June 2014
Phase: N/A
Study type: Observational

The study will obtain data to show insight into clinical outcomes of patients switching from Darbepoetin Alfa to a epoetin alfa biosimilar.

NCT ID: NCT02190461 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Impact of Early Respiratory Rehabilitation in the Exacerbations of Re-admitted COPD Patients

Start date: April 2013
Phase: N/A
Study type: Interventional

Open clinical trial with 1 year follow up comparing the impact of an Early Respiratory Rehabilitation program with the conventional Respiratory Rehabilitation in COPD re-admitted patients. Outcomes will be exacerbations, symptoms, functional capacity and quality of life related to health (HRQOL).