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NCT ID: NCT00421785 Recruiting - ESRD Clinical Trials

Effect of N-Acetylcysteine on Peritoneal Membrane Function in Chronic Peritoneal Dialysis Patients

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

The aim of our study is to investigate the effect of N-acetylcysteine on peritoneal small solute clearance and removal of salt and water in prevalent CAPD patients.

NCT ID: NCT00421577 Not yet recruiting - Caries Clinical Trials

Technique for Localization of Caries Associated Bacteria on Tooth Surfaces.

Start date: n/a
Phase: N/A
Study type: Observational

There is a simple laboratory technique for localization of caries associated bacteria on tooth surfaces by taking an impression of the teeth with a material containing sucrose. The purpose of this study is to check whether the technique can be incorporated into dental clinics as diagnostic tool comparing to other diagnostic methods available.

NCT ID: NCT00421369 Completed - Clinical trials for Major Depressive Disorder

Augmentation of the Antidepressant Action of Sertraline With Triiodothyronine (T3)and Reboxetine: Clinical Efficacy, Adverse Effects and Predictors of Response.

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

In this project we aim to further refine indications for the use of the thyroid hormone - T3 for patients suffering from depression. We aim to identify a sub-group of patients who are more likely to respond to T3 and establish the time in the treatment course when T3 should be added. The results of this project could have significant, direct clinical implications.

NCT ID: NCT00421265 Not yet recruiting - Prostate Cancer Clinical Trials

Active Surveillance for Prostate Cancer With Indolent Features

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Observational

In patients with prostate cancer with indolent features, disease progrssion may be very slow and in many cases will never become clinically evident during the patient's lifetime. Active surveillance is a continuous process of monitoring disease characteristcs aiming to avoid the morbidity of active therapy in patients with stabe indolent parameters, while offering early detection of disease activity in others who will need active therapy to control their disease. We hypothesize that active surveillance will permit the avoidance of therapy related morbidity in the majority of appropriate patients and will be associated with maintaining their quality of life.

NCT ID: NCT00421161 Not yet recruiting - Dermatitis Clinical Trials

Olive Oil With Omega 3 to Treat Stasis Dermatitis

Start date: January 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Olive oil and Omega 3 have many anti inflammatory effects that may be beneficial in the inflammation and edema of chronic stasis dermatitis. The olive oil contains many mono unsaturated fatty acids and anti oxidants that may add to the well being of a diseased skin by improving cell membrane homeostasis.

NCT ID: NCT00420394 Recruiting - Stomach Neoplasms Clinical Trials

Perioperative Chemoradiotherapy for Potentially Resectable Gastric Cancer

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

Rationale: Adjuvant chemoradiation considered as standard of care after curative surgery for adenocarcinoma of stomach and gastroesophageal cancer. Preoperative chemotherapy in the in locally advanced gastric cancer results in significant tumoral downstaging with improved rate of curative resections. Purpose: To evaluate feasibility and safety of combination of preoperative chemotherapy and postoperative chemoradiation for locally advanced adenocarcinoma of stomach and gastroesophageal cancer

NCT ID: NCT00420212 Completed - Clinical trials for Relapsing-Remitting Multiple Sclerosis

Efficacy and Safety of Oral BG00012 in Relapsing-Remitting Multiple Sclerosis

DEFINE
Start date: January 2007
Phase: Phase 3
Study type: Interventional

To determine if treatment with BG00012 can decrease the number of MS relapses during a certain time period. To determine if, over time, BG00012 treatment can decrease the number of certain types of brain lesions commonly seen in MS patients and slow down the time it takes for the disease to get worse. The purpose of this study is also to determine the safety of BG00012 and how well it is tolerated. Another goal is to see what effect BG00012 may have on tests and evaluations used to assess MS.

NCT ID: NCT00420069 Withdrawn - Clinical trials for Blood Gas Monitoring, Transcutaneous

Biphasic Extrathoracic Cuirass Ventilation During Dental Treatment

Start date: July 2008
Phase: N/A
Study type: Observational

The MRTX portable lightweight respirator (MRTX) provides noninvasive respiratory support using biphasic extrathoracic ventilation via a cuirass fitted around the patient's chest.The aim of the study is to evaluate the efficacy of the MRTX during dental treatment under deep sedation in comparison with the conventional treatment where children are only under monitor and only intervention is done when required.Twenty healthy children (ASA1) will wear the cuirass. PO2 saturation and ETCO2 will be recorded as a baseline. Half of the children will be ventilated (with similar values to those of physiologic respiration) and the other half will notThe study is blind, since the anesthesiologist and the dentist would not know if the cuirass of the child is connected to the MRTX or not: Group 1- 10 children with the cuirass will be connected to the MRTX and artificially ventilated at pressures of (-12/+5) at a rate of 20 per minute, and PO2 and ETCO2 will be recorded every 5 minutes. Group 2- 10 children with the cuirass will not be connected to the MRTX, but the machine will work at the same condition. Same records of PO2 and ETCO2 will be registered.

NCT ID: NCT00419874 Recruiting - Clinical trials for Traumatic Brain Injury

Characteristics of Blood- Brain Barrier Permeability in Neurological Patients

Start date: n/a
Phase: N/A
Study type: Observational

The main goal of the present study is to challenge the hypothesis that blood- brain barrier disruption following brain injury increases the risk for long-term disability, development of brain dysfunction, epileptic seizures and neuroanatomical alterations.

NCT ID: NCT00419627 Not yet recruiting - Ovarian Cancer Clinical Trials

Proteomic Analysis of HLA Complex in Solid Cancers: Breast, Ovary, Colon, Rectum, Stomach, and Pancreas

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

The purpose of this study is to evaluate the presence of proteins in solid tumors which may lead to an immune response