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NCT ID: NCT01592630 Withdrawn - Clinical trials for Colorectal Disorders

Effectiveness of Transverse Abdominus Plane Catheter Blocks to Patient-controlled Analgesia in Laparoscopic Colon Resections

Start date: May 2012
Phase: Phase 3
Study type: Interventional

The control of postoperative pain has become a major issue in surgery awareness and it is considered an important measurement of patient satisfaction. Improvements in pain relief, including stopping pain before it starts (i.e. preemptive treatment) is of great benefit to the surgical patient. When pain is aggressively addressed, patients respond by recovering faster. The use of opioids remains the mainstay to minimize postoperative pain. Lately, long acting local anesthetic wound infiltration has been widely recognized as a useful adjunct to multimodal postoperative pain management. On that basis, a system that delivers a continuous local anesthetic to the surgical wound was developed, and better pain control has been achieved after several surgical procedures. In patients undergoing abdominal procedures, such as colon resection, adequate pain control remains an issue. It is known that innervation to the antero-lateral abdomen is provided by sensory nerves T7-L1, ilioinguinal and iliohypogastric nerves, which travel through the transverse abdominis muscle plane (TAP). Local anesthetic block of these nerves has been described and has shown to be effective for immediate postoperative pain control. Recently, the use of the On-Q pain relief system with catheters placed within the TAP has been evaluated. Published results have shown significant improvement of pain control (Forastiere). The idea of placing the pain catheters at the TAP plane seems to be more coherent with the anatomical distribution of the sensory nerves trunks. Due to the lack of prospective trials investigating the effectiveness of a continuous wound infusion with local anesthetics after general surgery procedures the investigators sought to determine the efficacy of this technique after laparoscopic colon resection procedures.

NCT ID: NCT01592487 Withdrawn - Brain Function Clinical Trials

Effects of a Breakfast and Snack on Cognitive Function in Preadolescents

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

This study is designed to test how breakfast affects brain function, memory and learning in healthy children. Hypotheses: Based on the results of our initial study and the relevant literature, it is hypothesized that arousal, attention, and performance will be: 1. Greater in those who eat breakfast relative to those who do not; 2. Greater in lean than in overweight children receiving the higher protein breakfast; 3. Greater in fasting lean than fasting overweight children; and 4. Improved following a morning snack in all study groups. 5. Poorer in children with higher stress-related measures (e.g., higher cortisol levels). 6. Heart rate will be lower in fasting relative to fed participants, and across groups will be higher in overweight children.

NCT ID: NCT01591759 Withdrawn - Clinical trials for Traumatic Brain Injury

A Pilot Trial of Citicoline in Individuals With Mild Traumatic Brain Injury (mTBI)

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

This investigation will explore the impact of 8 weeks of citicoline treatment on cognitive function, clinical state and substance use in 40 individuals with mild traumatic brain injury (mTBI).

NCT ID: NCT01591291 Withdrawn - Alcoholism Clinical Trials

Pharmacogenetic Treatments for Alcoholism

Start date: June 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Heavy drinking can cause serious health, family, and economic problems. Finding treatments that are effective in decreasing heavy drinking among alcohol-dependent individuals is, therefore, an important scientific and health goal. A novel and important strategy to enhance alcoholism treatment efforts uses a personalized medicine approach to optimize treatment effects by selecting the "right" patient therapeutically and potentially with a minimum of adverse events, for a specific medication. This study will extend findings from a randomized double-blind clinical trial of ondansetron, in which the medication was found to reduce drinking among individuals with certain genotypes (i.e., forms of DNA, the material that controls the inheritance of characteristics). The proposed study will address a number of limitations in the prior work, including testing the medication in both European-American and African-American samples.

NCT ID: NCT01589718 Withdrawn - Clinical trials for Proliferative Diabetic Retinopathy

A Study of the Safety, Tolerability, and Efficacy of IVT Pre-op 0.3mg Pegaptanib Sodium Versus Sham, for Management of Tractional Retinal Detachment and Vitreous Hemorrhage With Proliferative Diabetic Retinopathy

No-Crunch01
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess whether preoperative pegaptanib sodium safely improves vitreous hemorrhage prior to surgical intervention and to evaluate the stability of pre-existing tractional retinal detachment.

NCT ID: NCT01589081 Withdrawn - Nicotine Dependence Clinical Trials

Effects of Progesterone on IV Nicotine-Induced Changes in Hormones and Subjective Ratings of Stimulant Drug Effect

Start date: September 2008
Phase: N/A
Study type: Interventional

The proposed clinical studies will analyze the interactions between progesterone, nicotine, alterations in endocrine hormones, mood and cardiovascular measures. It is hypothesized that the administration of progesterone at a dose that mimics luteal phase levels in normal cycling women will diminish the positive subjective effects of nicotine, as has been consistently observed for cocaine. This novel approach could have direct implications for facilitating smoking cessation treatment in women of reproductive age

NCT ID: NCT01589068 Withdrawn - Nicotine Dependence Clinical Trials

Effects of Progesterone on IV Nicotine Induced Changes on BOLD fMRI Signal, Hormones and Subjective Ratings of Stimulant Drugs

Start date: January 2007
Phase: N/A
Study type: Interventional

The proposed clinical studies will analyze the interactions between progesterone, nicotine, fMRI measures of patterns of brain activity, covariance with endocrine hormones, mood and cardiovascular measures. It is hypothesized that the administration of progesterone at a dose that mimics luteal phase levels in normal cycling women will diminish the positive subjective effects of nicotine, as has been consistently observed for cocaine. This novel approach could have direct implications for facilitating smoking cessation treatment in women of reproductive age

NCT ID: NCT01589055 Withdrawn - Nicotine Dependence Clinical Trials

IV Nicotine Induced Changes in Hormone Function, Mood States and Behavior

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

Clinical studies are proposed to analyze the interactions between nicotine, alterations in endocrine hormones, mood and cardiovascular measures. The studies are designed to examine the contribution of gender and menstrual cycle phase. It is hypothesized that analysis of nicotine's rapid hormonal, cardiovascular and subjective effects will be important for developing novel biologic approaches to treatment for nicotine abuse and dependence as well as advancing understanding of the neurobiology of nicotine reinforcement.

NCT ID: NCT01588340 Withdrawn - Hydronephrosis Clinical Trials

MRI Hydronephrosis Study

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

The purpose of this study is to compare a rapid noncontrast MRI protocol not requiring sedation to ultrasound in the assessment of hydronephrosis.

NCT ID: NCT01588314 Withdrawn - Neuropathic Pain Clinical Trials

Safety and Efficacy of Gabapentin for Neuropathic Pain in Fabry Disease

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

The purpose of this study is to determine efficacy of gabapentin vs. placebo at controlling peripheral neuropathic pain in patients with Fabry disease, and reducing their use of opioid analgesics. The investigators are conducting a randomized, double-blind, placebo controlled, single center, cross-over study. The primary endpoint is percent reduction in patients' use of hydrocodone-acetaminophen.