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NCT ID: NCT00181753 Withdrawn - Burns Clinical Trials

Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition

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

The purpose of the study is to understand how the body uses amino acids in burned patients during the time they cannot eat normally. Amino acids occur naturally in the body and the food we eat. The body combines amino acids to make protein. It uses the proteins to do things such as heal wounds, fight infection, and provide energy. We are studying two ways of receiving nutrition: through a vein or through a tube. We are also studying two different types of food: with or without glutamine. The results of this study will be used to determine the best type and way to supply nutrients during a severe burn injury. We hope to learn how to help the body use nutrients more efficiently to better repair wounded tissues and recover earlier from injury.

NCT ID: NCT00181649 Withdrawn - Lactation Clinical Trials

Recombinant Human Prolactin for Lactation Induction

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The purpose of the study is to assess the safety and determine the effects of the hormone prolactin on lactation (breast milk production).

NCT ID: NCT00179842 Withdrawn - Crohn Disease Clinical Trials

Immune Ablation and Stem Cell Support for Crohn's Disease

Start date: n/a
Phase: Phase 2
Study type: Interventional

The investigators anticipate that this study will also form the basis to clarify further the role of the immune system in Crohn's disease.

NCT ID: NCT00179192 Withdrawn - Clinical trials for End-Stage Renal Disease

Prevention and Treatment of Hemodialysis Vascular Access Malfunction

Start date: May 1998
Phase: Phase 2
Study type: Interventional

Vascular access is considered the Achilles heel of the dialysis patient. It constitutes the largest single cause of morbidity in the chronic hemodialysis population, accounting for over 25% of hospitalizations at an estimated cost in the US of at least one billion dollars annually. Currently, complication free survival of vascular access ranges between 30-50% a year and multiple investigative efforts in this area have been initiated and are directed at prolonging the functional life of vascular accesses. It is not well established whether intervention prior to overt malfunction or thrombosis of the vascular access could reduce these complications and thereby improve the functional longevity of the access. Moreover, once accesses at potential risk are identified, it is not well established which method of intervention, Surgery vs. Angioplasty vs. Expectant Management, is superior in terms of clinical and financial outcome. The proposed study aims to determine whether early intervention of a vascular access determined to be at risk of malfunction and thrombosis improves the long term outcome and, specifically, which means of intervention is preferred.

NCT ID: NCT00178854 Withdrawn - Clinical trials for Treatment Resistant Depression

Risperidone (Risperdal) Augmentation in Depressed Partial Responders to SRI Treatment

Start date: May 2004
Phase: Phase 4
Study type: Interventional

This is a study of the chemistry of depression in people who are taking an antidepressant but it is not working well. The changes in brain chemicals that occur when an SSRI type antidepressant is supplemented with risperidone (Risperdal®) will be studied. Spinal fluid is used to measure chemical levels of dopamine, serotonin, and other chemicals thought to be involved in depression. The study has potential to help understand and treat depression.

NCT ID: NCT00178750 Withdrawn - Pain Clinical Trials

"Loss of Resistance" Versus CompuFlo® for Epidural Placement

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to compare how well the CompuFlo® computerized syringe pump works as compared to the traditional method of inserting an epidural (a needle placed in one's back to give pain medicine).

NCT ID: NCT00178451 Withdrawn - Carotid Stenosis Clinical Trials

Stroke Prevention With Abciximab in Carotid Endarterectomy

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

In the first portion of the study, the goal will be to determine the safety of the drug Abciximab for use during and in the period after open carotid artery surgery. In addition, using specialized ultrasound equipment (a probe that is placed on the outside of your skin of your head), we will aim to measure the number of particles released around the time of surgery while being treated with Abciximab. The second phase of the study will be determine if Abciximab can safely reduce the number of particles released into the bloodstream around the time of surgery in order to reduce the risk of stroke.

NCT ID: NCT00178438 Withdrawn - Crohn's Disease Clinical Trials

Wireless Capsule Endoscopy in Small-Bowel Crohn's Disease

Start date: June 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the best role for capsule endoscopy in diagnosing Crohn's disease.

NCT ID: NCT00178321 Withdrawn - Critically Ill Clinical Trials

Improving Sleep in the Pediatric Intensive Care Unit

Start date: September 2005
Phase: N/A
Study type: Interventional

Sleep is disrupted in the PICU. This disruption has been reported in studies that have used: (a) observation of sleep-wake cycles (b) self-reports by children themselves , and (c) objective measures (e.g., electroencephalograph( EEG). Noise and light levels have been correlated with profound sleep disruption in the PICU . Sleep disruption is known to have a profound impact on the overall health of a child, both from a physiological and a psychological standpoint . In addition, sleep disruption has been shown to change cortisol levels, cause impaired immune responses and impair cognitive function in both children and adults . Disruption in sleep also is known to impair healing through these many complex connections with other homeostatic processes in the human body. What is the effect of wearing earplugs in critically ill children admitted to the PICU on: 1. Sleep states 2. Physiological stability (e.g. melatonin, cortisol and immune status) 3. Sleep habits after discharge from the PICU (on the general pediatric unit, 2 weeks and 2 months after discharge), and 4. Child behavior at 2 weeks and 2 months after discharge from the PICU by parent report on the Child Behavior Checklist (CBCL).

NCT ID: NCT00177879 Withdrawn - Clinical trials for Cognitive Deficits Related to Internet Use

Usability of a Website for People With Schizophrenia

Start date: August 2005
Phase: N/A
Study type: Interventional

This study will determine the usability of a website for people with schizophrenia versus other websites designed for the same purpose.