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NCT ID: NCT00910312 Completed - Fibroadenoma Clinical Trials

ICE-SENSEā„¢ Cryotherapy for Breast Fibroadenoma Trial

ICE-CRYSTAL
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Ice-Sense, a novel cryotherapy system (a system that freezes tissues), is safe and effective in the treatment of benign breast tumors such as fibroadenoma.

NCT ID: NCT00909376 Not yet recruiting - Pregnancy Clinical Trials

Is Early Second Trimester Vaginal Ultrasound Scan Associated With Adverse Perinatal Outcomes?

Start date: July 2009
Phase: N/A
Study type: Observational

Many pregnant women have an ultrasound done of their fetus in the beginning of the second trimester of pregnancy. Some have a transvaginal sonography while others have a transabdominal one, depending on clinical parameters such as weight, scars etc. In the transvaginal ultrasound there is some amount of version of the fetus done by the examiner to maintain a better aspect of the fetus, while this is not done in a transabdominal sonography. The objective of this trail is to determine whether having a transvaginal ultrasound as opposed to a transabdominal one has an association to adverse perinatal outcomes.

NCT ID: NCT00909285 Completed - Clinical trials for Alzheimer Disease, Early Onset

Effects of Transcranial Magnetic Stimulation (TMS) and Cognitive Training for Alzheimer Patients

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

Current diagnosis of Alzheimer disease is made by clinical, neuropsychological, and neuroimaging assessments. Routine structural neuroimaging evaluation is based on nonspecific features, such as atrophy, which is a late feature in the progression of the disease. Therefore, developing new approaches for early and specific recognition of Alzheimer disease at the prodromal stages is of crucial importance. In the present study the investigators would like to examine if combined treatment with TMS and cognitive training (CoTra) for several weeks can produce a sustained improvement in cognitive and behavioral symptomatology of Alzheimer's disease (AD) patients. A number of in vivo neuroimaging techniques, which can be used to reliably and noninvasively assess aspects of neuroanatomy, chemistry, physiology, and pathology, hold promise.

NCT ID: NCT00908518 Not yet recruiting - Clinical trials for Cognitive Dysfunction

The Difference in Postoperative Cognitive Dysfunction and Myocardial Ischemia Between Propofol and Isoflurane

POCD
Start date: June 2009
Phase: N/A
Study type: Observational

The progressive aging of the general population cause increase in number of extensive and long surgeries in older patients. Age is a risk factor for perioperative myocardial ischemia and Postoperative Cognitive Dysfunction (POCD) The suggested study will deal with the above-mentioned complication in patients older then 65 years undergoing major non-cardiac surgeries. It has been shown that Isoflurane and sevoflurane may have a cardio-protective effect after cardiac surgery involving cardio-pulmonary bypass, and it was recommended that isoflurane should be used in these cases. A question was raised but haven't been answered yet, whether this cardio-protective effect exists also in non-cardiac major surgery. The aim of this study is to evaluate whether there is a difference in the occurrence of postoperative cognitive dysfunction and perioperative myocardial ischemia between total intravenous anesthesia using propofol and isoflurane based anesthesia.

NCT ID: NCT00908505 Not yet recruiting - Cystic Fibrosis Clinical Trials

Comparison Between RTX (Biphasic Cuirass Ventilator) and Physiotherapy in Cystic Fibrosis Patients

RTX
Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness of different mucous clearance techniques in cystic fibrosis patients

NCT ID: NCT00908063 Terminated - Clinical trials for Traumatic Brain Injury

Safety and Tolerability of Oxycyte in Patients With Traumatic Brain Injury (TBI)

STOP-TBI
Start date: October 2009
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the safety and tolerability of a single administration of Oxycyte in patients with severe non-penetrating traumatic brain injury (TBI). In the first dose level (Cohort 1), 11 patients were randomized 2:1 to receive either 1.0 mL/kg Oxycyte (0.6 g/kg; n=8) or NS (n=3). A total of 8 patients received Oxycyte. The Data Safety Monitoring Board (DSMB) reviewed the safety data for patients in Cohort 1 through Day 14, and approved escalation to the next dose. In Cohort 2, 18 patients will be randomized 2:1 to receive either 2.0 mL/kg Oxycyte (1.2 g/kg; n=12) or NS (n=6). The DSMB will then review the safety data for all patients in Cohort 2 through Day 14 and either approve escalation to the highest dose or remain at the current dose. If remaining at the current dose level (Cohort 2) an additional 50 patients will be randomized 1:1 to Oxycyte (n=25) or NS (n=25) and treated. If escalation occurs to Cohort 3, 18 patients would be randomized 2:1 to Oxycyte (n=12) or NS (n=6) to receive the 3.0 mL/kg dose. The DSMB would again review the safety data and decide whether to treat an additional 50 patients at this dose or to decrease the dose back to 2.0 mL/kg. This group would be randomized 1:1 to receive Oxycyte (n=25) or NS.

NCT ID: NCT00907998 Completed - Clinical trials for Coronary Heart Disease

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of APL180

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

The design of this study will enable an extensive evaluation of safety, tolerability, and PK-PD relationship following 4 weeks of dosing in patients with Coronary heart Disease

NCT ID: NCT00907712 Withdrawn - Clinical trials for Diagnostic Techniques, Cardiovascular

Cardiovascular Assessment Before and After Limb Amputation

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

Vascular lower limb amputees have an increased morbidity and mortality. The aim of the study is to evaluate the hemodynamic changes after amputation and its relation to outcome.

NCT ID: NCT00907491 Completed - Cough Clinical Trials

Accuracy of Cough Detection in Healthy Adults

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

Cough is part of the defense mechanism to protect the lung from foreign particles and remove secretions from the airways. However, at times it becomes a bothersome, annoying symptom that interferes with the quality of life, sleep pattern and exercise tolerance of the patient. People with respiratory infection, asthmatic patients and CF patients suffer from a multitude of pathologies of airways and are often inflicted with chronic cough. Treatment of cough in these patients consists of many types of expectorants, cough suppressors, secretion modifiers, inhaled bronchodilators etc. In addition, chest physical therapy (PT) is often prescribed as part of the treatment regime. The primary objective of the study is to evaluate the efficacy and validity of novel cough counting device based on the WIM Technology.

NCT ID: NCT00906620 Completed - Depression Clinical Trials

Saving and Empowering Young Lives in Europe (Israel)

SEYLE-ISRAEL
Start date: September 2009
Phase: Phase 0
Study type: Interventional

SEYLE is a health promoting program for adolescents in European schools. Its main objectives are to lead adolescents to better health through decreased risk-taking and suicidal behaviors, to evaluate outcomes of different preventive programs and to recommend effective culturally adjusted models for promoting health of adolescents in different European countries. Because of the significance of the SEYLE program and the importance of suicide research, Israel is honored to take part in this program and be a collaborator in it's implementation and research.