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NCT ID: NCT01167985 Recruiting - Clinical trials for Irreversible Pulpitis

A Clinical Study: the Antibacterial Effect of Insoluble Antibacterial Nanoparticles (IABN) Incorporated in Dental Materials for Root Canal Treatment

IABN
Start date: July 2013
Phase: Phase 2
Study type: Interventional

The effect of Antibacterial Nanoparticles, Incorporated in root canal sealer material and in provisional restoration is going to be examined. Two different tests are planned: (1) clinical and radiological evaluation of root canal sealer.(2) An evaluation in the laboratory the efficacy of provisional restoration during root canal treatment.We assume, based on our previous laboratory studies that show antibacterial properties, that the incorporation of the nanoparticels will improve the treatment outcome.

NCT ID: NCT01167686 Recruiting - Clinical trials for Respiratory Infections

Effects of Gardemont S.A Food Supplement on Upper Respiratory Illness

Start date: March 2010
Phase: Phase 2
Study type: Interventional

General:Prospective, randomized, double blind controlled trial of the food supplement GOLDTRAIN PLUS, to assess its safety and efficacy in comparison to placebo in subjects with upper respiratory infection. Hypothesis: The food supplement GOLDTRAIN PLUS will be superior to placebo in shortening the time to recovery from the disease symptoms. Study design and outcome measures:Study population of 182 generally healthy subjects with acute respiratory infection randomized in 1:1 ratio to active supplement versus placebo treatment, with randomization stratified by site. The study supplement administration will be continued for 7 days, and patient global assessment (PGA) will be the main primary measurement tool, based on a self-reporting questionnaire filled and monitored every 12 hours for 7 consecutive days. Throat and nasal swabs determining type of viral infection, will be taken at inclusion of patient and a number of blood tests at the end of treatment to look for any adverse effects of the medication. Analysis and conclusion: All data-from the filled questionnaires, clinical follow up and laboratory studies will be analyzed by multivariate analysis to determine the efficacy of the supplement and its correlation to the clinical and laboratory parameters.

NCT ID: NCT01167673 Recruiting - Clinical trials for Irritable Bowel Syndrome

The Effect of Coltect (Selenium, Curcumin and Green Tea) on Irritable Bowel Syndrome

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

Irritable bowel syndrome (IBS) causes many symptoms, including abdominal pain, irregular bowel movements and bloating. It may be caused by loe degree inflammation of the intestine. The ingredients of coltect which contains green tea, selenium, and curcumin have been proven very safe and have anti inflammatory and anti oxidant activity. The aim of the study is to see whether the use of Coltect can improve symptoms in IBS patients.

NCT ID: NCT01167660 Recruiting - Clinical trials for Blood Coagulation Tests

Non Invasive Measurement of Coagulation in Term and Preterm Neonates

Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this study is to assess the reliability of a new non-invasive device to assess the blood coagulation status among term and preterm babies.

NCT ID: NCT01167647 Completed - Tuberculosis Clinical Trials

The Role of Routine Bacterial Culture Including Tuberculosis During Bronchoscopy: A Prospective Study

Start date: July 2010
Phase: N/A
Study type: Observational

Many centers routinely culture bronchoscopy samples for bacteria and mycobacteria even when infections including tuberculosis (TB) are not strongly suspected. However, the value of this practice has been poorly defined.

NCT ID: NCT01167439 Recruiting - Dysphagia Clinical Trials

Dysphagia in Oculopharyngeal Muscular Dystrophy (OPMD)- Evaluation, Endoscopic Examination of Swallowing, Treatment and Long Term Follow up

OPMD
Start date: July 2009
Phase: Phase 1
Study type: Interventional

The investigators aimed to review the natural history of dysphagia and dysphonia in OPMD in order to identify the best candidates and the proper timing to perform dysphagia alleviating procedures in both heterozygote and homozygote patients from the large pool of cases with this disease in Israel.

NCT ID: NCT01165918 Not yet recruiting - Clinical trials for Normal Healthy Embryos

Derivation of New Human Embryonic Stem Cell Lines: Identification of Instructive Factors for Germ Cells Development

Start date: October 2010
Phase: N/A
Study type: Observational

The purpose of this study is 1. To generate human embryonic stem cells lines (hESC) lines 2. Study of the factors that contribute to differentiation towards germ cell.

NCT ID: NCT01165879 Recruiting - Pregnancy Clinical Trials

Measuring Uterine Electrical Activity Throughout Pregnancy and Labor Measuring Uterine Electrical Activity Throughout Pregnancy and Labor

Start date: May 2010
Phase: N/A
Study type: Observational

The EUM100pro (Electrical Uterine Monitor)is a uterine contraction monitor which measures uterine contractions based on the electrical activity of the uterine muscle.The study will compare the EUM100pro measurements to the already existing uterine contractions monitors (tocodynamometer and Intra Uterine Pressure Catheter) in pregnant women with complaints of uterine contractions.

NCT ID: NCT01165814 Completed - Pain Clinical Trials

Naproxen Versus Tramadol for Post Cesarean Pain Control

Start date: August 2006
Phase: N/A
Study type: Interventional

Oral naproxen might be more efficacious for post-cesarean pain-control and have better side-effects profile than oral tramadol.

NCT ID: NCT01164345 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Mozobil for Autologous Stem Cell Mobilization

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate Plerixafor (MOZOBIL) plus recombinant human G-CSF (G-CSF) efficiency in mobilizing sufficient number of stem cells from Lymphoma (NHL and HL) patients for autologous transplantation.