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NCT ID: NCT01979666 Terminated - Clinical trials for Necrosis, Avascular, of Bone

Nitrate Patch Use as Treatment of Knee AVN

Start date: January 2014
Phase: N/A
Study type: Interventional

The pathogenesis of AVN includes a defective blood supply to the knee joint. Local nitrates induce peripheral vasodilation and may improve blood supply to the affected tissue. This study aims to test whether the use of a nicotine patch may accelerate the healing process from AVN of the knee.

NCT ID: NCT01979042 Completed - Acute Renal Failure Clinical Trials

Urinary Markers for Unilateral Kidney Obstruction

Start date: October 2013
Phase: N/A
Study type: Observational

Renal colic is usually caused from an obstructing stone along the ureter. Some of the patients present with a high level of creatinin in the blood, even though there is a normal functioning contralateral kidney. Furthermore creatinin is not an ideal marker for renal function during acute changes. Several works have shown that modern urinary markers such as NGAL (neutrophil gelatinase-associated lipocalin), KIM-1 (Kidney Injury Molecule-1) and others rise earlier and are much more sensitive for kidney insult. There is a lack of research on their role in acute kidney obstruction

NCT ID: NCT01978938 Completed - cUTI Clinical Trials

Efficacy and Safety Study of Eravacycline Compared With Levofloxacin in Complicated Urinary Tract Infections

Start date: October 6, 2014
Phase: Phase 3
Study type: Interventional

This is a phase 3, randomized, double-blind, double-dummy, multicenter, prospective study to assess the efficacy and safety of eravacycline compared with levofloxacin in participants with complicated urinary tract infections (cUTI).

NCT ID: NCT01978860 Completed - Clinical trials for Chronic Total Occlusion of Coronary Artery

A Prospective, First in Man Study to Evaluate the Safety and Performance of the NovaCross™ Micro-catheter

Start date: November 2013
Phase: N/A
Study type: Interventional

This is a prospective, non-randomized, first-in-man investigational study, to assess the safety and technical feasibility, deployment and withdrawal characteristics of the NovaCross™ micro-catheter during an interventional coronary angioplasty procedure and evaluating the CTO penetration rate. Each study subject/patient will have a total of one (1) procedure performed for this study.

NCT ID: NCT01978769 Completed - ADHD Clinical Trials

The Effect of Physical Effort in the Decision Making Process of Preadolescents With ADHD

Start date: November 2014
Phase: N/A
Study type: Observational

In the current study we will examine a specific aspect of these processes that has yet to be studied. We will test the effect that a physically effortful assignment has on the choices that a preadolescent makes using a forced choice paradigm in which the participant will be asked to choose between and carry out either a high cost-high reward option (HR) or a low cost-low reward (LR) option. The HR option will demand a significant amount of physical effort and will be paired up with a large reward as opposed to the LR option which will be less demanding physically and paired up with a small reward. The assignment will be carried out using a hand held dynamometer which measures the power produced by the participants' upper extremity. We propose that a child with attention deficit hyperactivity disorder (ADHD) will choose a task that involves less effort despite the small reward tied to it compared to a control child who will choose the more demanding task and the larger reward.

NCT ID: NCT01978340 Withdrawn - Clinical trials for Sleep Apnea, Obstructive

Eval EarlySense Bet Lowenstein Sleeplab

Start date: November 2013
Phase: N/A
Study type: Observational [Patient Registry]

The study objective is to collect heart rate, respiration rate and motion data of patients admitted to sleep lab and to determine the accuracy level of the EarlySense system vs. the monitors used in sleep lab (e.g., Polysomnography, respiratory belts, ECG, etc..) . Data regarding sleep condition, scoring and quality of sleep and in and out of bed status, patient turns will also be collected and compared to data collected by EarlySense contactless monitor. Different patient population will be monitored including obese, morbidly obese, patients with or without obstructive/central apnea, patients with or without arrhythmia as well as healthy population who arrive to sleep lab for general evaluation will be monitored

NCT ID: NCT01977833 Recruiting - Type 2 Diabetes Clinical Trials

Meal Timing on Postprandial Glucose, Insulin and GLP-1 in Type 2 Diabetes

GLP-1inT2D
Start date: October 2013
Phase: N/A
Study type: Interventional

Enhanced insulin and GLP-1 postprandial response after morning meal versus evening meal, might be underlying explanation of the beneficial effect of eating breakfast with reduced dinner vs skipping breakfast on glycemic control and HbA1c in T2D patients. To test this hypothesis and clarify whether glucose, insulin and GLP-1 postprandial responses are different in the morning vs. in the afternoon, the investigators will compare in T2D subjects in random order and in two separate days: the glucose, insulin and GLP-1 postprandial responses after breakfast, lunch and dinner with 2 isocaloric meal plans or test diets, that differ in meal timing distribution The investigators hypothesize that GLP-1 and insulin response after high calorie breakfast will be higher in comparison to GLP-1 and insulin response after identical meal at evening

NCT ID: NCT01977651 Completed - Clinical trials for Metastatic Castration-resistant Prostate Cancer (mCRPC)

A Study to Evaluate the Potential Increased Risk of Seizures Among Metastatic Castration-Resistant Prostate Cancer (mCRPC) Patients Treated With Enzalutamide

UPWARD
Start date: September 25, 2013
Phase: Phase 4
Study type: Interventional

The objective of this study was to evaluate the incidence of seizures and monitor the safety of enzalutamide treatment in participants with metastatic castration-resistant prostate cancer (mCRPC) known to have risk factor(s) for seizure.

NCT ID: NCT01977547 Completed - Anemia Clinical Trials

Age of Blood in Children in Pediatric Intensive Care Units

ABC-PICU
Start date: January 2014
Phase: Phase 3
Study type: Interventional

ABC PICU is a randomized clinical trial that will compare the clinical consequences of RBC storage duration in 1538 critically ill children. Laboratory and observational evidence points to serious concerns about the lack of safety and effectiveness of older RBCs, especially in more vulnerable populations. Physicians and institutions have been systematically transfusing fresh RBCs to some pediatric patients primarily because of beliefs that the use of fresh RBCs improve outcomes. Conversely, the standard practice of blood banks is to deliver the oldest RBC unit in order to decrease blood wastage. To provide much needed high quality evidence to answer the question "do RBCs of reduced storage duration improve outcomes?" The ABC PICU Trial will conduct a RCT comparing development of New or Progressive Multiple Organ Dysfunction Syndrome (NPMODS) in critically ill children transfused with either RBCs stored ≤ 7 days or standard issue RBCs (expected mean RBC storage duration of 17-21 days).

NCT ID: NCT01977404 Not yet recruiting - Clinical trials for Congestive Heart Failure

Nutritional Evaluation of Patients With Congestive Heart Failure

Start date: November 2013
Phase: N/A
Study type: Observational

This study objective is to assess the nutritional status of Patients With Congestive Heart Failure.