Clinical Trials Logo

Filter by:
NCT ID: NCT01633450 Completed - Healthy Clinical Trials

Zinc Absorption From Biofortified Rice

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

One of the newest strategies to combat micronutrient deficiencies is the biofortification of staple foods, where higher levels of minerals are obtained through breeding of staple crops. The aim of this study is to evaluate zinc absorption from a rice biofortified with zinc when compared with a control rice fortified with zinc just before consumption.

NCT ID: NCT01632774 Completed - Aortic Rupture Clinical Trials

Analysis of Risk Factors for Death After Blunt Traumatic Rupture of the Thoracic Aorta

Start date: January 1990
Phase: N/A
Study type: Observational

Aortic injuries after blunt thoracic trauma are compared to the great incidence of accidents relatively rare, but potentially serious leading to death at scene in most of the cases. The study was undertaken to delineate mortality and its risk factors on three different levels (pre-hospital, in-hospital and overall). Between 1990 and 2003, all consecutive patients and victims with traumatic aortic rupture were retrospectively analyzed by reviewing hospital and autopsy records.

NCT ID: NCT01632631 Completed - Clinical trials for Infrarenal Aortic Aneurysm

Patient-specific Virtual Reality Rehearsal Prior to EVAR: Influence on Technical and Non-technical Operative Performance

Start date: September 2012
Phase:
Study type: Observational

Ongoing technological advances, especially in the field of image processing, have refined medical simulations to offer life-like replications of medical and surgical procedures in a variety of specialties. Patient-specific image data are incorporated into these simulations, and transformed into a 3D model. This enables the practitioner and his/her team to perform and practice 'real' cases on a virtual patient prior to performing the real procedure on the actual patient. This new technology has been referred to as 'patient-specific' rehearsal, also 'mission' or 'procedure' rehearsal. Research has already proven that simulated patient-specific rehearsal of a carotid artery stenting procedure may enhance surgical and team performance. The PROcedure rehearsal software can now also be used to practice patient-specific endovascular repair of infrarenal aortic aneurysms (EVAR). The ability to rehearse a challenging and complex procedure like EVAR may not only influence device selection based on preoperative planning, but also improve the technical performance of the surgeon/radiologist and the awareness and communication within the entire endovascular team. However, further research is needed to evaluate if this new technology may enhance clinical safety and efficiency, i.e. if patients actually benefit from physicians and team members conducting patient-specific rehearsals of EVAR interventions.

NCT ID: NCT01632228 Completed - Glioblastoma Clinical Trials

A Study of Onartuzumab (MetMAb) in Combination With Bevacizumab Compared to Bevacizumab Alone or Onartuzumab Monotherapy in Participants With Recurrent Glioblastoma

Start date: June 29, 2012
Phase: Phase 2
Study type: Interventional

This randomized, double-blind, placebo-controlled, multicenter phase II study will evaluate the safety and efficacy of onartuzumab in combination with bevacizumab as compared to bevacizumab alone in participants with recurrent glioblastoma. Participants will be randomized 1:1 to receive either placebo plus bevacizumab every 3 weeks, or onartuzumab plus bevacizumab. Study treatment will continue until disease progression, unacceptable toxicity, participants or physician decision to discontinue, or death.

NCT ID: NCT01632124 Recruiting - Clinical trials for Rheumatoid Arthritis

Rituximab-induced Pulmonary Function Changes

Start date: January 2012
Phase: N/A
Study type: Observational

Measuring lung function (FVC, FEV1, DLCO) before, during and after treatment with rituximab in patients with rheumatoid arthritis or inflammatory myositis.

NCT ID: NCT01632111 Completed - Fabry Disease Clinical Trials

Pulmonary Involvement in Patients With Fabry Disease

Start date: July 2012
Phase: N/A
Study type: Observational

The objective of this study is to investigate whether Agalsidase alpha, a drug commonly prescribed in patients with Fabry disease, is associated with improvement of the pulmonary involvement. According to the Global Initiative for Obstructive Lung Disease (GOLD), the surrogate markers for obstructive lung diseases are a decrease in both forced expiratory volume in one second (FEV1) and FEV1/FVC ratio, whereas FVC is the forced vital capacity. However, the measurement of these lung function parameters is indicated as yearly follow-up examinations with or without the treatment of Agalsidase alpha in patients with Fabry disease.

NCT ID: NCT01631110 Completed - Influenza Clinical Trials

Re-licensing Study to Assess Inflexal V Formulated With WHO Recommended Influenza Strains

Start date: July 2012
Phase: Phase 3
Study type: Interventional

The study is to assess whether the influenza vaccine Inflexal V for season 2012/2013 fulfills the EMA requirements for re-registration of influenza vaccines.

NCT ID: NCT01631071 Completed - Influenza Clinical Trials

Re-licensing Study to Assess Virosomal Influenza Vaccine Formulated With WHO Recommended Influenza Strains

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

The study is to assess whether the virosomal influenza vaccine for season 2012/2013 fulfills the EMA requirements for re-registration of influenza vaccines.

NCT ID: NCT01630785 Enrolling by invitation - Clinical trials for Patients Operated on at the Neurosurgery Department

Neurophysiological Intraoperative or Epilepsy Monitoring

nphysdocu
Start date: January 2012
Phase:
Study type: Observational [Patient Registry]

The investigators record the outcome of patients whose surgery involved intraoperative neurophysiological monitoring - Trial with surgical intervention

NCT ID: NCT01629264 Completed - Pregnancy Clinical Trials

The Influence of Hormonal Changes During Pregnancy on Corneal Biomechanics in Humans

Start date: June 2012
Phase: N/A
Study type: Observational

The intraocular pressure in the human bulbus requires that the "wall" of the eye shows a certain (bio)mechanical strength. The human cornea represents the anterior portion of this wall. Since several years, there is a growing interest in the ophthalmological community for identifying factors modulating the biomechanical stability of the human cornea. Reasons are twofold: advances in keratoconus research and the increasing numbers of refractive laser surgery procedures with (correspondingly) increasing numbers of complications due to non-respecting the limits of corneal biomechanics. There is evidence that oestrogen, but also thyroïd hormone changes have a major impact on corneal biomechanics. A number of recent observational studies have reported on keratoconus and refractive laser surgery patients with decompensating biomechanics during pregnancy. Both hormones also show physiological changes during pregnancy and little is known about the impact of these physiological changes on the human cornea. The aim of this study is to establish baseline values for physiological changes in the human cornea during pregnancy.