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NCT ID: NCT00307983 Recruiting - Malnutrition Clinical Trials

Effect of Malnutrition on the Prognosis in Hemodialysis Patients

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

The purpose of this study is to examined the effect of malnutrition and/or inflammation on atherosclerosis and prognosis in hemodialysis.

NCT ID: NCT00319397 Recruiting - Aging Clinical Trials

Effects of Age and Exercise on Blood Pressure Regulation

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

The purpose of this study is to investigate the effects of age, exercise and cardiovascular disease on blood pressure.

NCT ID: NCT00416065 Recruiting - Cancer Clinical Trials

PET/CT to Identify "Vulnerable" Arterial Plaque

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

The purpose of this research is to evaluate the presence, location and intensity of FDG uptake in the large arteries using the new technology of fused PET/CT imaging and to compare FDG uptake with the presence of arterial calcifications as seen on the simultaneously acquired CT, in order to determine if FDG was increases incalcified plaque or in a different location in the arterial wall. we will also evaluate the relationship between FDG localization and future cardiovascular events in out patient population

NCT ID: NCT00633802 Recruiting - Clinical trials for Borderlone Personality Disorder

Low-Dose Risperidone Treatment for Subjects Suffering From Borderline Personality Disorder

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

Personality disorders are life-long maladaptive behavioral patterns. Borderline personality disorder (BPD) is the leading personality disorder encountered in clinical settings, often associated with tremendous distress. It is characterized by impulsivity, emotional lability, unstable interpersonal relationships, with particular sensitivity to abandonment. BPD patients are prone to self destructive behaviors and all too frequently attempt suicide. When in emotional turmoil, persons with BPD may also develop brief, transient psychotic states. Psychotherapy for BPD is a common treatment option, but it requires considerable time and specific personnel training, and is therefore not always feasible. Medical treatment is an efficacious alternative, however there is no concensus on drug selection. Some experts have suggested that medical treatment should be selected individually according to the subject's dominant clinical symptom. Several psychopharmacological groups have been proposed: Antidepressants, mood stabilizers, and several novel antipsychotic drugs. The latter are particularly promising since they may produce symptomaic improvement with fewer adverse effects. Risperidone has been shown in a few preliminary studies to be promising in the treatment of various BPD symptoms, but no controlled study has tested it yet. We propose to test the efficacy of risperidone in the treatment of BPD in a double-blind crossover design using both clinical and phsysiological measure.The main hypothesis is that risperidone will be efficient in alleviating BPD core and secondary symptoms.

NCT ID: NCT01430884 Recruiting - Clinical trials for Coronary Heart Disease

Analysis of Human Coronary Aspirate

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

During elective percutaneous coronary intervention (PCI), both proximal and distal protection devices are used. The distal occlusion protection device temporarily occludes the vessel distal to the lesion during the intervention, thereby capturing both particular debris and soluble substances released from the lesion such that they can be aspirated and prevented from reaching the coronary microcirculation. Rather than simply discarding the material which is retrieved from use of protection devices, the investigators have recently taken advantage of this situation, sampled the particulate and soluble material and subjected it to a variety of analyses with the ultimate goal to have a better insight into the respective plaque composition and to correlate it to the individual imaging and clinical data. On the basis of such information the investigators aim to better understand the pathophysiology of plaque vulnerability and to possibly predict the clinical development of the individual patient.

NCT ID: NCT01571531 Recruiting - Spinal Cord Injury Clinical Trials

European Multicentre Study of Human Spinal Cord Injury

Start date: April 2004
Phase:
Study type: Observational

Today there is accumulating evidence from animal experiments that regeneration can be induced after a spinal cord injury (SCI). Consequently in the near future, new therapeutic approaches to induce some regeneration will be included in the treatment of patients with SCI. The aim of this proposal is to provide the required clinical basis for the implementation of novel interventional therapies. The establishment of combined clinical, functional and neurophysiological measures for a qualitative and quantitative assessment of spinal cord function in patients with SCI at different stages during rehabilitation represents a basic requirement to monitor any significant effect of a new treatment. Therefore, several European Paraplegic Centres involved in the rehabilitation of acute traumatic SCI patients build up a close collaboration for standardised assessment. The aim is to get knowledge about the natural recovery after spinal cord lesion in a larger population of patients in the sense of a historical control group and to bring new standardised assessment tools to the clinical setting.

NCT ID: NCT01615549 Recruiting - Cholecystitis Clinical Trials

Efficacy of Proficiency-based Versus Free Laparoscopic Training in Cholecystectomy on a Virtual Reality Simulator

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

Virtual reality devices are widely accepted tools to familiarize surgical novices with the principles of laparoscopy. Free Virtual reality training will be tested against basic training and efficacy assessed in a randomized controlled trial of surgical novices.

NCT ID: NCT02321423 Recruiting - Clinical trials for Pachyonychia Congenita

International Pachyonychia Congenita Research Registry

IPCRR
Start date: April 2004
Phase:
Study type: Observational [Patient Registry]

International Pachyonychia Congenita Research Registry (IPCRR) is a patient registry for those suffering from Pachyonychia Congenita (PC). PC is an ultra-rare extremely painful skin disorder that causes painful blisters and callus on feet and sometimes hands, thickened nails, cysts and other features. The IPCRR consists of a questionnaire, patient photos, optional physician notes from telephone consultation to validate questionnaire and free genetic testing.

NCT ID: NCT02634086 Recruiting - Clinical trials for Coronary Artery Disease

Long-term Outcome of Triple-vessel Coronary Artery Disease Underwent Three Different Strategies (LOTUS)

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

The study is to determine the long-term outcome of patients with coronary triple vessels disease (TVD) in the real world of China, by three different treatment strategies: percutaneous coronary intervention (PCI), Coronary artery bypass graft (CABG) or optimal medication therapy (OMT).

NCT ID: NCT02901392 Recruiting - Clinical trials for Urinary Incontinence, Stress

Fundación IVO Registry for Patients Undergoing Sling or Artificial Urinary Sphincter After Prostate Cancer Treatment

Start date: April 2004
Phase:
Study type: Observational [Patient Registry]

Stress urinary incontinence is a significant potential source of morbidity after radical prostatectomy or radiation therapy for prostate cancer. At present, artificial urinary sphincter remains the preferred therapeutic option. However, this technique is not free from complications. In an attempt to avoid such complications, male sling has been suggested for use in patients with mild degrees of stress incontinence.