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NCT ID: NCT01427569 Completed - Diabetic Foot Ulcer Clinical Trials

Efficacy Study of IZN-6D4 Gel for the Treatment of Diabetic Foot Ulcers

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if topical application of a hydrogel that contains plant extracts will improve healing of diabetic foot ulcers when compared to treatment with a hydrogel alone.

NCT ID: NCT01426984 Recruiting - Clinical trials for Borderline Personality Disorder

A Double Blind Crossover Study on the Effect of MPH on Decision-making Ability of Adults With BPD Compared to Adults With ADHD and Healthy Adults

Start date: May 2012
Phase: N/A
Study type: Interventional

The study assesses the effect of Ritalin on working memory,attention,and decision-making measures in adults with BPD and compares it to its effect on healthy adults and adults with BPD (using data form study SHA 01-10), in a double-blind crossover design. The investigators hypothesize that Ritalin will result in better performance in all measures.

NCT ID: NCT01426932 Enrolling by invitation - Vertigo Clinical Trials

The Head Impulse Test in the Screening of Vestibular Function

Start date: October 2011
Phase: N/A
Study type: Observational

The alternate binaural bithermal caloric test (ABBT) is a well established examination in the evaluation of the dizzy patient. ABBT is useful in detecting the side of peripheral vestibulopathy by stimulating each ear separately, it contributes to the diagnosis of bilateral vestibular involvement when all responses to cold and warm stimuli are reduced, and adds to the differentiation of peripheral from central vestibular involvement by measuring the fixation-induced inhibition of the caloric response. In spite of these benefits, ABBT is the most time-consuming part of the electronystagmography/Videonystagmography (ENG/VNG) test battery, and frequently causes significant inconvenience to the patient due to the repeated extreme vestibular stimuli. The head impulse test (HIT) assesses vestibular function by brisk, passive rotations of the head in the plane of the examined semicircular canals. Whenever the vestibulo-ocular reflex (VOR) is deficient, this maneuver would produce catch-up saccades aiming to the re-fixation of the eyes on the target. Hence, both residual VOR and catch-up saccades act synergistically to stabilize gaze. The HIT requires only several minutes and might cause minimal discomfort only. The study hypothesis is that the HIT recorded by standard VNG equipment of the VNG system would provide diagnostic information on the side of vestibular involvement matching that of the ABBT.

NCT ID: NCT01425619 Completed - Anxiety Disorder Clinical Trials

The Effect of Medical Clowns and Topical Anesthetic Cream on Pain and Anxiety in Children Undergoing Allergy Skin Tests

Start date: October 2011
Phase: N/A
Study type: Interventional

Allergy skin tests are occasionally associated with pain and anxiety in patients undergoing this procedure. The investigators intend to examine if medical clowns compared with local anesthetic cream can decrease these feelings in children.

NCT ID: NCT01425606 Not yet recruiting - Clinical trials for Hyponatremia of Multiple Myeloma

Pseudohyponatremia of Multiple Myeloma is True Hyponatremia

Start date: September 2011
Phase: Phase 4
Study type: Observational

Hypothesis: the hyponatremia of multiple myeloma (m.m.)is true and not pseudohyponatremia by using the stewart approach to acid - base interpretation, would like to show that the positive charged m- proteins produced in m.m.result in true hyponatremia.

NCT ID: NCT01425593 Recruiting - Chronic Urticaria Clinical Trials

T Cell Function in Chronic Idiopathic Urticaria

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

Chronic idiopathic urticaria (CIU) is a common form of chronic urticaria in which the cause is not detected after intensive clinical and laboratory investigation.In view of the current data, it was suggested that at least part of the patients with CIU have an autoimmune process.This study is designed to investigate the mechanisms involved in the regulation and activation of the immune cells in patients with CIU and corelate them with disease activity

NCT ID: NCT01425359 Completed - Clinical trials for Coronary Artery Disease

Type 2 Diabetes Evaluation of Ranolazine in Subjects With Chronic Stable Angina

TERISA
Start date: September 2011
Phase: Phase 4
Study type: Interventional

This study will evaluate the effect of ranolazine compared to placebo on the average weekly angina frequency in subjects with chronic stable angina and coronary artery disease (CAD) who have a history of type 2 diabetes mellitus (T2DM), and whether ranolazine can reduce the frequency of angina (chest pain) attacks, compared to a placebo. Subjects will be asked to record their daily angina episodes in a diary at the end of each study day. Ranolazine is approved for the treatment of chronic angina, and is not approved for the treatment of T2DM.

NCT ID: NCT01425255 Withdrawn - Type 1 Diabetes Clinical Trials

The Impact of Continuous Glucose Monitoring Use on Sleep in Parents of Children With Type 1 Diabetes Mellitus

Start date: August 2011
Phase: N/A
Study type: Observational

The purpose of this prospective exploratory study is to compare sleep quality and sleep-wake patterns in parents of children with type 1 diabetes (T1D) before and several weeks after initiating using real-time continuous glucose monitoring (RT-CGM) of their children.

NCT ID: NCT01424566 Completed - Pain Clinical Trials

A Two-Part Study of Sativex® Oromucosal Spray for Relieving Uncontrolled Persistent Pain in Patients With Advanced Cancer

Start date: June 29, 2012
Phase: Phase 3
Study type: Interventional

The primary objective of this study was to evaluate the efficacy of nabiximols (Sativex®), compared with placebo, when used as an adjunctive measure in relieving uncontrolled persistent chronic pain (not breakthrough pain) in participants with advanced cancer, who had inadequate analgesia even with optimized chronic opioid therapy. This multi-center study was conducted in two parts. All participants enrolled into the trial received nabiximols during one of two parts of the study, but they did not know which part. Eligible participants were not required to stop any of their current treatments or medications.

NCT ID: NCT01423942 Completed - Clinical trials for Analysis, Event History

Maturation of the Autonomic Nervous System in Prematures

Start date: October 2011
Phase: N/A
Study type: Observational

The purpose of this study is to try to evaluate the maturation of the autonomic nervous system in prematures.