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Petach Tikva, Israel Clinical Trials

A listing of Petach Tikva, Israel clinical trials actively recruiting patients volunteers.

RESULTS

Found (345) clinical trials

A Naturalistic Study of the Efficacy and Safety of Escitalopram in Treatment Resistant Depression

The primary objective of this multicenter study is to evaluate the efficacy of escitalopram in treatment resistant depression (TRD), assessed by 2 consecutive failed antidepressant treatments from different classes. The last treatment received is a 6 week prospective trial with venlafaxine.

Phase N/A

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The Israeli Trigger for Blood Transfusions in the ICU

Anemia is a common problem in critically ill patients admitted to intensive care units (ICUs). The etiology is multifactorial and includes sepsis, overt or occult blood loss (including frequent blood sampling), decreased production of endogenous erythropoietin, and immune-associated functional iron deficiency. In the only large randomized trial addressing the issue …

Phase N/A

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The Impact of Right Ventricular Pacing on Tricuspid Regurgitation

"1" Traditionally, tricuspid regurgitation in the presence of pacemaker is attributed to the physical interference of the valve closure by the electrode. "2" Right ventricular pacing may be associated with dyssynchrony in contraction of the right ventricular wall (i.e. septum and free wall. "3" The tricuspid sub-valvar apparatus is anchored …

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Firazyr Patient Registry (Icatibant Outcome Survey - IOS)

The Icatibant Outcome Survey (IOS) is a multicenter, prospective, observational study for participants treated with Firazyr (icatibant) and/or Cinryze (C1 inhibitor [human]) in countries where it is currently approved. The entry of participants in the Icatibant Outcome Survey (IOS) is at the discretion of the physician and the participant and …

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Evaluation of the Tyto Thermometer When Used in Clinical Care Setting

Patients who present to the Emergency Department will be evaluated for eligibility to the study. Those meeting all the inclusion criteria and none of the exclusion criteria will undergo an informed consent process and will sign a written consent. Within each age group both afebrile and febrile patients will be …

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Direct Oral Anticoagulants Pharmacodynamics in Octogenarian Patients With Atrial Fibrillation

A cross sectional, prospective study of hospitalized and ambulatory patients, who are treated with DOACs for AF. Patient population Candidate for the study will be patients older than 80 years (octogenarians) and those 70 years who are 1) admitted to the Internal Medicine division in Rabin Medical Center or to …

Phase N/A

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Entyvio (Vedolizumab) Long Term Safety Study

The drug being tested in this prospective, observational study is called vedolizumab. Vedolizumab is being used to treat people who have UC or CD. This study will look at the long-term safety of vedolizumab versus other biologic agents in participants with UC or CD. The study will enroll approximately 5000 …

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The Influence of Obesity on Level of Depression and Cognitive and Executive Functions

The proposed study is a randomized, open, comparative research involving an intervention group and two control groups. The aims of the study are: 1.To compare levels of depression in female adolescents with obesity and a control group of female adolescents with appropriate weight and height. 2. To investigate whether a …

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Evaluation of the Benefits for Overall Health Following Cochlear Implant Treatment in the Elderly Population

The study is designed as an observational prospective repeated measures study with each subject acting as his/her own control. Subjects are evaluated subjectively at pre- and post-operative intervals that coincide with their routine visits to the clinic. Outcomes from routine practice and application of cochlear implant intervention are recorded through …

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VelaShape and Contour I V3 for Abdominal Fat Reduction vs. Control

Eligible subjects will undergo one treatment on one abdominal subarea. Another abdominal subarea will remain without treatment and will serve as a control. Biopsies from treated and untreated areas will be harvested during abdominoplasty and cultured.. Treatment with VelaShape will be performed to arm 1, and treatment with Contour I …

Phase N/A

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