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NCT ID: NCT00749164 Not yet recruiting - Clinical trials for Graft-Versus-Host Disease

Allogeneic Mesenchymal Stem Cell for Graft-Versus-Host Disease Treatment

MSCGVHD
Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Now it is commonly accepted that MSC produce an immune-tolerant environment in different settings. It has been shown (mainly for BM-MSC) that MSC can down-regulate T cells activation. This characteristic of BM derived MSC already has clinical implications and shows their potent effectiveness both in prophylaxis and treatment of resistant GvHD. Ongoing clinical trials of use bone marrow MSC for treatment of steroid resistant GvHD are successfully run on and some bone marrow donor registries included BM-MSC as a material for donation. According to our preclinical studies MSC from cells from marrow, placenta, umbilical cord vessels demonstrate similar pronounced immunosuppressive effect both with autologous and allogeneic lymphocytes. Our preliminary clinical experience shows that BM-MSC is an effective tool for treatment of steroid resistant GVHD. Present study aimed to demonstrate if human UC-MSC has in vivo immunosuppressive effect and can be used for GVHD treatment

NCT ID: NCT00748722 Active, not recruiting - Clinical trials for Breast Reconstruction

Pre-Operative Imaging of Abdominal Wall Perforators Using CT Angiography

DIEP
Start date: September 2008
Phase: N/A
Study type: Observational

Abdominal donor-site flaps, including the transverse rectus abdominis musculocutaneous (TRAM) and deep inferior epigastric artery perforator flaps(DIEP), are standard in autologous breast reconstruction. With significant variation in the vascular anatomy of the abdominal wall, preoperative imaging is essential for preoperative planning and reducing intraoperative error. The quest continues for optimal preoperative assessment. Computed tomographic angiography has recently been proposed as a noninvasive modality for this purpose. It provides the location of the perforator vessels, diameter and anatomic course in regards to the rectus muscle. In this study we will perform preoperative lower abdominal computed tomographic angiography in DIEP flap breast reconstruction patients.

NCT ID: NCT00748384 Completed - Clinical trials for Age Related Macular Degeneration

Usability of the Foresee Home in Intermediate Age Related Macular Degeneration (AMD) Patients

UU2
Start date: February 2009
Phase: N/A
Study type: Observational

The study purpose is to demonstrate that the target population can receive a packed FORESEE HOME unpack it, install and operate it to an extent that the FORESEE HOME can monitor them for changes in the visual field with good specificity. And evaluate the device usage on a small scale, at the subjects' homes before a commercial use.

NCT ID: NCT00747760 Completed - Hypothyroidism Clinical Trials

TSH Receptor Mutations Among a Consanguineous Community

TSHR
Start date: December 2005
Phase: N/A
Study type: Observational

Resistance to thyrotropin (RTSH) is a condition of impaired responsiveness of the thyroid gland to TSH, characterized by elevated TSH, low or normal thyroid hormone levels, and hypoplastic or normal-sized thyroid gland. The aim of the present study was to evaluate the clinical course over time,the genotype-phenotype association and the frequency of two different TSH-receptor (TSHR) mutations in a highly consanguineous population of the town of Um-El-Fahem.

NCT ID: NCT00747513 Completed - Obesity Clinical Trials

A Multi-component Program to Reduce Obesity in Children

Start date: September 2009
Phase: N/A
Study type: Interventional

In an attempt to challenge the increasing prevalence of childhood obesity, many programs have been executed in order to improve childrens' lifestyle. Programs involved either school, family or environmental measures. In most, success was only limited. The purpose of this trial is to examine the ability of a low-cost multi-component program to improve behavioral, diet and activity habits in both school, family and afternoon settings. Ths ultimate goal is to construct and assess a lifestyle modification program that can be implemented in schools and kindergartens on a national level. Participants will be ~2,500 children aged 5-12 from 22 kindergartens and elementary schools, divided into control and intervention centers. Teachers and students will be provided with materials in order to perform activities on healthy food and drink choices and habits during the school day. Schools will offer increased physical activity opportunities to children, as will afternoon community centers. Children will be given personal exercise items. Parents will be offered lectures on topics of diet and activity. Diet and activity habits will be assessed by a questionnaire, and height, weight and body fat percentage will be measured before and after the program.

NCT ID: NCT00747071 Withdrawn - Clinical trials for Clostridium Difficile-Associated Diarrhea

Safety and Validation of Efficacy of Oral Administration of the Food Additive Colostrum Derived Anti Clostridium Difficile Antibodies

Start date: September 2011
Phase: Phase 2/Phase 3
Study type: Interventional

This clinical study is designed to evaluate the safety and efficacy of oral administration of the food additive colostrum derived antibodies to Clostridium difficile for prevention of Clostridium difficile associated disease (CDAD).

NCT ID: NCT00746915 Recruiting - Pain Clinical Trials

Phase I Study Evaluating The Safety And Efficacy of a Device for Collection of Electrical Bioimpedance Data

Start date: March 2009
Phase: Phase 1
Study type: Interventional

The objectives of this study are to evaluate the safety and initial efficacy of the epidural injection procedure when combined with real-time multi-frequency bio-impedance measurements that collect data on the electrical bioimpedance characteristics of living human tissue on the path of the epidural needle.

NCT ID: NCT00746707 Completed - Clinical trials for Grade 1 Perineal Tears

Biologic Glue for First Degree Perineal Tears

Start date: September 2008
Phase: N/A
Study type: Interventional

The use of octyl-2-cyanoacrylate adhesive glue is not inferior to traditional suturing for first degree perineal tears repair

NCT ID: NCT00746642 Not yet recruiting - Diabetes Mellitus Clinical Trials

Use of Mellitor Sensor for Continuous Glucose Monitoring - An Ex-Vivo Study

Start date: October 2009
Phase: N/A
Study type: Interventional

Most patients with diabetes mellitus have to measure their blood glucose levels quite often, in order to maintain a proper glycemic control. Current methods of self-monitoring of blood glucose are invasive, painful, uncomfortable, and only allow occasional, from time-to-time, measurements. Real-time continuous monitoring would provide a helpful tool for improvement of glycemic control, thus decreasing the incidence of hypoglycemia and improving glucose control. The Mellitor sensor is a new concept of continue glucose monitoring device. The Mellitor device is an implantable continuous glucose monitoring sensor that is intended for detection episodes of hyperglycemia and hypoglycemia in diabetic patients, and facilitates both acute and long-term therapy adjustments. This study was design in order to evaluate glucose measurement capabilities by the Mellitor sensor that is being developed. Transudate liquid samples, withdrawn in a clinical procedure and normally immediately disposed, will be used for glucose measurement by the Mellitor sensor. Study Design This study is an ex-vivo comparative study. 20 patients will be recruited for the study, according to patients' inflow and meeting eligibility criteria. Study Goal Study objective is to evaluate the feasibility of the Mellitor Sensor technology for glucose level measurement. Study Endpoint Mellitor technology feasibility will be established by comparing Mellitor glucose measurements results, based on transudate/exudates liquid withdrawal for other medical reasons, to "gold standard, Yellow Springs" glucose analyzer, or a comparable, calibrated and approved device using the same transudate/exudates liquid. Interdevice variability should be within 10%.

NCT ID: NCT00746291 Terminated - Cerebral Palsy Clinical Trials

Heart Rate Variability (HRV) Among Children With Brain Damage

Start date: June 2008
Phase: N/A
Study type: Interventional

to investigate the function of the autonomic nervous system in children with with post traumatic brain injury and children with cerebral palsy through an analysis of heart rate variability (HRV) occurring with walking performance.