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NCT ID: NCT00727519 Completed - Clinical trials for End Stage Renal Disease

The Effect of Pomegranate Juice on Oxidative Stress in Hemodialysis Patients

Start date: July 2008
Phase: Phase 3
Study type: Interventional

Pomegranate juice (PJ) consumption by hemodialysis patients will reduce the oxidative stress and the incidence of infections, cardiovascular events and mortality.

NCT ID: NCT00726674 Completed - Type 2 Diabetes Clinical Trials

Basal Insulin for Type 2 Diabetes Patients Treated in Outpatient Clalit Clinics

Lapas II
Start date: August 2008
Phase: N/A
Study type: Observational

Treatment of diabetes mellitus type II with basal insulin, for patients treated in Clalit outpatient clinics that are not adequately controlled with current treatment.

NCT ID: NCT00726635 Recruiting - Ovarian Cancer Clinical Trials

The Assessment of Preoperative Psychological Intervention on Stress in Women With Gynecological Malignancies

Start date: August 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to asses the impact of a tailored preoperative psychological intervention on women with gynecological malignancies on psychological, physiological and immunological parameters

NCT ID: NCT00726245 Completed - Muscle Tear Clinical Trials

Plasma Rich in Growth Factors (PRGF) Treatment for Muscle Tear

Start date: January 2008
Phase: Phase 2/Phase 3
Study type: Interventional

the improvement of symptoms and disease progress by the treatment of OA of the knee with PRGF

NCT ID: NCT00725907 Completed - Soft Tissue Healing Clinical Trials

Treatment of ATFL Tears With PRP

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

PRP will enhance ATFL tears healing by time and quality.

NCT ID: NCT00725686 Completed - Clinical trials for Age-Related Macular Degeneration

Study of PF-04523655 (REDD14NP) In Subjects With Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (Wet AMD)

Start date: February 2007
Phase: Phase 1
Study type: Interventional

The aim of the study is to evaluate whether PF-04523655 is safe in the treatment of neovascular/wet AMD

NCT ID: NCT00725660 Not yet recruiting - Pregnancy Clinical Trials

Pre-Eclampsia Prediction By Doppler Screening Of Uterine Arteries And Angiogenic Factors In Second Trimester Of Pregnancy

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

BACKGROUND: Pre-eclampsia complicates about 2% of pregnancies. It accounts for at least 50 000 maternal deaths per year worldwide and is the second most common cause of maternal death in the developing world. Also, Pre-eclampsia is the commonest cause of iatrogenic prematurity, It frequently coexists with intrauterine growth restriction (IUGR) and placental abruption, other important causes of adverse prenatal outcome. There have been many studies investigating whether the disease can be prevented. In order to achieve this, one needs to be able to identify firstly those women that are at highest risk of the disease. Early studies showed that impedance to flow in the uterine arteries decreases with gestation in normal pregnancies, while in pregnancies with established pre-eclampsia or IUGR the impedance is increased. These observations led to a number of screening studies in the second trimester, which assessed if it is possible to predict those pregnancies destined to have complications of impaired placentation. These studies showed that women with increased impedance to uterine artery blood flow have an increased risk of developing pre-eclampsia, and detection can be further increased by using angiogenic factors (That are involved in the pathogenesis of Pre- eclampsia and could be useful for early prediction of the disease: VEGF, PIGF, PP13, sFLT1) in combination with uterine arteries Doppler study in the second trimester. METHODS: In this study we would like to add uterine arteries Doppler to the early routine detailed ultrasound examination (14-16 weeks), in 3000 women in Jerusalem. in addition we would like to check angiogenic factors from the serum blood taken for the routine triple test in these women (16-18 weeks).pregnancy outcome would be collected after labour from the medical centers participating in this research.

NCT ID: NCT00725569 Completed - Cesarean Section Clinical Trials

Homeopathy for Post-operative (C. Section) Recovery

Start date: August 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The planned study will be conducted in a prospective, randomized, double blind placebo controlled manner. Two "anti-traumatic" Homeopathic remedies (Arnica montana and Staphysagria) will be used. The selection of these remedies was based on a previous trial that showed a statistical difference in Hemoglobin levels favoring pregnant women treated with these drugs following delivery. The proposed study will focus on the post-operative recovery of women undergoing Cesarean section. According to Homeopathic principles, these two remedies are believed to improve the "vital force", and will therefore improve convalescence following surgery in the study group. The study will include 90 women between the ages of 18 and 50 years who are scheduled for elective Cesarean Section. Exclusion criteria are: obesity (above 100kg), malignancy, psychiatric illness, diabetes and multipara pregnancies. Participants will be inducted following a detailed explanation by an MD and signing of an informed consent form, and then subdivided randomly into three groups numbering 30 in each: Two groups will be treated with homeopathic drugs of varied doses, and the third will get a placebo remedy which is indistinguishable from the other drugs. Outcome measures will include: 1. Blood loss - as estimated by a reduction in serum Hemoglobin levels. 2. Pain -to be evaluated by a numerical rating score (NRS) 3. Analgesic use 4. Length of post-operative stay and complications. 5. Quality of life outcomes - to be assessed using the MOS SF-36 questionnaire at one and four weeks following surgery. Although not expected, adverse events will be monitored. If, as we anticipate, the homeopathic treatment proves to be both safe and effective in shortening the duration of post-operative healing, this will have significant implications, with respect to both healthcare costs and patient suffering. It will also open the door for further research in the field of trauma medicine, as well as other stress-related illness.

NCT ID: NCT00724802 Recruiting - Canavan Disease Clinical Trials

Oral Glyceryl Triacetate (GTA) in Newborns With Canavan

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

Canavan disease is caused by Aspartoacylase deficiency. There is no treatment for the disease, but there is a food additive that includes acetate . We suggest an early treatment with acetate and a neurologic evaluation, including MRI, after 4 months of treatment. In any case the treatment will be stopped at the age of 22 months, when myelinization is ended.

NCT ID: NCT00724503 Completed - Colorectal Cancer Clinical Trials

FOLFOX Plus SIR-SPHERES MICROSPHERES Versus FOLFOX Alone in Patients With Liver Mets From Primary Colorectal Cancer

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

This study is a randomized multi-center trial that will assess the effect of adding Selective Internal Radiation Therapy (SIRT), using SIR-Spheres microspheres®, to a standard chemotherapy regimen of FOLFOX as first line therapy in patients with non-resectable liver metastases from primary colorectal adenocarcinoma. Treatment with the biologic agent bevacizumab, if part of the standard of care at participating institutions, is allowed within this study at the discretion of the treating Investigator.