Clinical Trials Logo

Filter by:
NCT ID: NCT02392780 Not yet recruiting - Clinical trials for Acute-graft-versus-host Disease

Cannabidiol for the Treatment of Severe (Grades III/IV) Acute Graft-versus-host Disease

Start date: April 2015
Phase: Phase 2
Study type: Interventional

Graft-versus-host-disease (GVHD) is a major obstacle to successful allogeneic hematopoietic cell transplantation (alloHCT). Cannabidiol (CBD), a non-psychotropic ingredient of Cannabis sativa possesses potent anti-inflammatory and immunosuppressive properties. In a recent phase 2 study, CBD has been shown to be safe and reduced significantly the incidence of acute GVHD compared to control patients with a hazard ratio of 0.3. Based on these results the investigators propose a phase 2 study to explore the efficacy of oral CBD in the treatment of severe (grades III/IV) acute GVHD, a pathology with a dismal prognosis.

NCT ID: NCT02383836 Not yet recruiting - Clinical trials for Patent Foramen Ovale

Influence of Position on Detection of Patent Foramen Ovale by Simultaneous Transesophageal Echo and Transcranial Doppler

Start date: March 2015
Phase: N/A
Study type: Observational

Patients will have simultaneous Transesophageal Echo (TEE) and Transcranial Doppler (TCD) performed and a comparison of timing, sensitivity and intensity of intravenously injected bubbles will be determined.

NCT ID: NCT02370576 Not yet recruiting - Clinical trials for Depressive Disorder, Major

The Effect of Traumatic Childbirth on the Incidence of PTSD and Other Major Postpartum Psychopathology

Start date: March 2015
Phase: N/A
Study type: Observational [Patient Registry]

Determination of incidence and prevalence of PTSD and other types of psychopathology (such as anxiety and affective disorders) after traumatic birth experiences and elucidation of salient risk factors in the local population sample- by prospective follow-up.

NCT ID: NCT02369289 Not yet recruiting - Clinical trials for Bone Mineral Density

Bone Mineral Density in Israeli Female Vegans and Omnivores

Start date: March 2015
Phase: N/A
Study type: Observational

A vegan diet is more and more prevalent in the general population in Israel in recent years. There have been some concerens that a vegan diet may lack in bone-health related nutrients (such as calcium, protein and vitamin D), and therefore may cause a decreased bone mineral density. The study aims to compare bome mineral density and other biochemical bone health parameters in vegan and omnivore non-menopausal Israely females.

NCT ID: NCT02363569 Not yet recruiting - Clinical trials for Vaginal Bleeding During Pregnancy

The Prognosis of Early Pregnancy With Post Coital Bleeding

Start date: February 2015
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective study, where the investigators will monitor pregnant women at 4-23 weeks of pregnancy coming to the "Women- E.R." at "Meir" Hospital due to spontaneous -or after intercourse- bleeding or bleeding secretions. The women will fill out questionnaires regarding past illness, vaginal bleeding, and gynecologic history. Then they will undergo full examination including ultrasound. After discharge, the investigators will recommend to all the women who came due to bleeding or bleeding secretions to avoid intercourse for two weeks after the bleeding stops. Afterwards they will be monitored until their delivery date (filling questionnaires a month after coming to the E.R. and at the end of the pregnancy). After they give birth the investigators will assess the rate of pregnancy, obstetric and embryonic complications in each of the study groups.

NCT ID: NCT02357628 Not yet recruiting - Wounds and Injuries Clinical Trials

Effect of Regulated Oxygen-Enriched Negative Pressure Therapy (RO-NPT) On Soft Tissue Wound Repair

Start date: March 2015
Phase: N/A
Study type: Observational

The investigators believe that regulated oxygen-enriched negative Pressure Therapy (RO-NPT) will be beneficial in the reduction or elimination of anaerobic infection in hard-to-heal soft tissue wounds.

NCT ID: NCT02344914 Not yet recruiting - Clinical trials for Second Stage of Labor

Dental Support and the Second Stage of Labor Among Multiparous Women

Start date: June 2015
Phase: Phase 3
Study type: Interventional

To assess if the use of the dental support device( DSD) Laboraideā„¢ shortens the second stage of labor and decreased the rate of obstetrical interventions, and if it's use alleviate pain.

NCT ID: NCT02342106 Not yet recruiting - Infertility Clinical Trials

Assessment of Myeloid Cell Constitution in the Follicular Fluid of Women Undergoing In-vitro Fertilization

Start date: January 2015
Phase: N/A
Study type: Observational

The investigators will study the immune cell subpopulations in follicular fluid of patients undergoing In-Vitro Fertilization (IVF) treatment in our clinic. The investigators will corelate the presence of immature myeloid cells to the ovarian stimulation response as indicated by follicle stimulating hormone (FSH) and number of follicles or estradiol level developed on the day of human chorionic gonadotropin (hCG) administration.

NCT ID: NCT02340871 Not yet recruiting - Clinical trials for Neurological Diseases

Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases

NGS
Start date: March 2015
Phase: N/A
Study type: Observational

In Israel, because of special qualification in neurogenetics, during a 30 year career ,we have found, characterized and treated at least 13 novel neurological diseases. The genetic basis was elucidated with geneticist colleagues both in Israel and worldwide. The diseases we have found encompass all the fields of pediatric neurology including intellectual disability, epilepsy, muscle-nerve disorders, malformations of the brain, microcephaly, macrocephaly, cerebellar ataxia, chorea. dystonia, cerebral palsy and many other symptoms and signs. We are especially interested in consanguineous families, in whom the parents are first or second degree cousins. These families often bear autosomal - recessive diseases. If the family is informative - with 2 or more affected children - then with current genetic techniques there is a good chance of finding the causative gene to this specific disease. This is not only a theoretical - academic accomplishment. In practice, after discovering the gene, the family is given genetic counseling and in their further pregnancies the geneticists will examine either by preimplantation genetic diagnosis (PGD) or amniocentesis if the embryo is affected or not. In the early stages of the pregnancy if the embryo is indeed affected by the disease caused by the gene we have found and the religious official consents, genetic counseling can offer termination of pregnancy to the couple. Needless to say, we know the immense burden of an affected child on the family, community and society. The parents are guilt-ridden, the affected child draws extensive resources from educational, health and rehabilitation authorities. We can contribute to the well-being of the family and the clan (because many times the relatives are affected). We can perform sophisticated genetic studies such as Whole Genome Sequencing and Whole Exome Sequencing.After an informative family is recruited to the study, we will explain the aims of the research. The parents and eligible patients will sign informed consent forms, according to the local Helsinki Board. Blood samples will be taken in Israel, DNA extracted in the Israeli lab and then shipped coded to the researchers in USA or Germany. If the researchers will find a new gene the family will be notified and given appropriate genetic counseling. We will continue to follow and treat the family onwards.

NCT ID: NCT02336295 Not yet recruiting - Vegan Diet Clinical Trials

Developing and Validating a Food Frequency Questionnaires (FFQ) for the Vegan Population in Israel

Start date: February 2015
Phase: N/A
Study type: Interventional

The study aims to validate a Food Frequency Questionnaire (FFQ) designed specifically for the vegan population in Israel. The participants will complete the FFQ, and the data will be verified by evaluating the participants energy expenditure (by measuring BMR, body composition and daily activity) and conducting a 24-hour food interview.