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NCT ID: NCT01441531 Withdrawn - Clinical trials for Tourniquet-induced Pain

Efficacy of Gabapentin in Prevention of Tourniquet Pain and Hypertension

Start date: January 2012
Phase: Phase 0
Study type: Interventional

The purpose of the study is to find out if taking a dose of gabapentin 600 mg by mouth (po) before surgery will help prevent the development of tourniquet pain and hypertension while the tourniquet is inflated during orif of tibia fracture.

NCT ID: NCT01439685 Withdrawn - Cholangiocarcinoma Clinical Trials

Comparison of Biliary Stenting Alone vs. Stenting With Photodynamic Therapy (PDT) During ERCP

PDT
Start date: July 2011
Phase: N/A
Study type: Observational

This study entails retrospective and prospective review of data from a database protocol. Data gathered will be then analyzed for a set amount of patients. In this study, the investigators will compare biliary stenting vs. biliary stenting plus photodynamic therapy (PDT) and assess if PDT can improve quality of life and prolong survival.

NCT ID: NCT01439334 Withdrawn - Drug Abuse Clinical Trials

Multiple Behavior Screening, Brief Intervention and Referral to Treatment (SBIRT) Model of Drug Abuse in Primary Care

SBIRT
Start date: December 2009
Phase: N/A
Study type: Interventional

The primary purpose of this research is to develop and evaluate the short-term efficacy of an innovative multiple behavior screening, brief intervention and referral to treatment (MB-SBIRT) model using social images and future self-images to simultaneously link and reduce prescription and other co-occurring drug use behaviors among emerging adults in a primary care setting serving a racially and economically diverse community. The long term objective of this research is to cost-effectively reduce prescription and illicit drug abuse, along with alcohol and tobacco consumption, and improve health-related quality of life among high-risk emerging adults often ignored in intervention research and services.

NCT ID: NCT01438671 Withdrawn - Distorted; Balance Clinical Trials

Wii Fit Balance Training Compared to Traditional Balance Training in Patients With SCI/TBI/CVA

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

Our hypothesis is the investigators will find a significant advantage for the use of a virtual reality system like the Wii Fit to improve overall balance scores versus the use of traditional balance activities alone. The objectives will be to determine the enjoyment of these types of gaming activities through the use of a survey to support the hypothesis that these activities are more enjoyable than traditional activities and to gather evidence to support the use of these more enjoyable activities as a viable and needed addition to the overall balance regimen given in the plan of care for a patient with traumatic or acquired brain injury, stroke or spinal cord injury.

NCT ID: NCT01438372 Withdrawn - Clinical trials for Inflammatory Bowel Disease

IV Iron Sucrose vs Oral FeSO4 in Treating IDA in Pediatric IBD

Start date: November 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of intravenous iron sucrose in comparison to oral ferrous sulfate in improving iron deficiency anemia in children with inflammatory bowel disease.

NCT ID: NCT01438242 Withdrawn - Clinical trials for Major Depressive Disorder

An Open Label Study of the Geneceptâ„¢ Assay in Treatment Resistant Depression

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the potential impact of the assay in terms of depression severity as measured by change in Clinical Global Impressions (CGI) scale at 3 months.

NCT ID: NCT01438047 Withdrawn - Port Wine Stain Clinical Trials

Optical Frequency Domain Imaging (OFDI) in Dermatology

Start date: September 2010
Phase: N/A
Study type: Observational

This is a pilot exploratory study. The goal of this study is to evaluate a new imaging tool, optical frequency domain imaging (OFDI), to reveal the microvascular morphology of capillary malformations.

NCT ID: NCT01435564 Withdrawn - Physical Activity Clinical Trials

Pilot Study: Mobile Phone Based Physical Activity in Sedentary Men and Women

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

The purpose of this pilot study is to estimate the efficacy of a mobile phone based physical activity intervention in sedentary men and women.

NCT ID: NCT01433770 Withdrawn - Clinical trials for Kidney Transplantation

Alefacept in Kidney Transplant Recipients

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

Alefacept, also known as Amevive®, is a medication approved by the Food and Drug Administration (FDA) in the United States and other countries for the treatment of psoriasis, which is a chronic inflammatory immunological skin condition that can result in chronic dry, red patches that are covered in scales. Alefacept is approved by the FDA for the treatment of psoriasis but not as an anti-rejection medication in transplant patients. It is now being tested in new kidney transplant patients as a supplement to other approved anti-rejection drugs. Alefacept will be used as an investigational drug in this study. The reason for this study is to test whether using Alefacept will inhibit T cells, known as memory cells, using a test named ELISPOT-IFN. In patients with psoriasis, Alefacept inhibits these memory cells. If memory cells specific to your donor can be inhibited by this drug, it might prevent rejection and promote acceptance of the transplanted kidney in a unique manner.

NCT ID: NCT01433718 Withdrawn - Clinical trials for Anterior Cruciate Ligament Injury

Decreasing Knee Injury Risk Factors With Neuromuscular Training

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

Anterior cruciate ligament (ACL) tears are disabling injuries that place a significant burden on the athlete. Roughly 80% of these injuries are linked to a noncontact mechanism, with more than 70% of them occurring while landing from a jump. Female athletes are at higher risk of sustaining a noncontact ACL injury due to the higher number of risk factors that they possess compared to their male counterparts. Due to this statistic, ACL prevention programs have been developed over the past 15 years in attempt to reduce this risk among the female athletic population. These programs have been shown to reduce the rate of noncontact ACL injuries in females by correcting the risk factors associated with them. However, it remains unclear as to whether these positive results are solely due to the program or a higher exercise workload in its participants. The purpose of this study is to evaluate the effectiveness that an ACL prevention program has on modifying at-risk landing mechanics (associated with noncontact ACL injury) compared to a resistance training program of equal workload.