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Wounds and Injuries clinical trials

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NCT ID: NCT01994148 Recruiting - Clinical trials for Gastrointestinal Injury

Application of Laparoscopy in Gastrointestinal Injury

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

laparoscopy has been increasingly applied in patients with abdominal trauma , as an diagnostic and therapeutic modality. However, its clinical benefits are still under evaluation. The aim of this study is to prospectively assess the feasibility and safety of this technique in the management of traumatic gastrointestinal injury.

NCT ID: NCT01983475 Recruiting - Osteoporosis Clinical Trials

Denosumab Administration After Spinal Cord Injury

Start date: January 2015
Phase: Phase 4
Study type: Interventional

Sublesional bone loss after acute spinal cord injury (SCI) is sudden, progressive, and dramatic. After depletion of bone mass and the loss of architectural integrity, it may be difficult, if even possible, to restore skeletal mass and strength. Denosumab is a relative new, highly potent anti-resorptive agent that has proven efficacy in postmenopausal osteoporosis to improve bone mass and in solid tumor patients to prevent a skeletal-related event to a greater extent than that with bisphosphonate administration. In persons with complete motor lesions, bisphosphonates have not been effective at reducing bone loss at the knee, the site of greatest relevance because of its increased risk of fracture. Anti-RANKL therapy appears to be more potent than bisphosphonates in animal models of bone loss due to immobilization, suggesting that treatment with denosumab may prove to be an efficacious therapy for persons with acute SCI to preserve bone mass and strength.

NCT ID: NCT01964859 Recruiting - Wounds and Injuries Clinical Trials

Feasibility Study for Fibroblast Autologous Skin Grafts

Start date: January 7, 2015
Phase: Phase 2
Study type: Interventional

This research is being done to determine if investigators can change skin from one type to another. Specifically, investigators are interested in making normal skin into the thicker skin found on our palms and soles.

NCT ID: NCT01957358 Recruiting - Spinal Cord Injury Clinical Trials

Resolving Grief After Spinal Cord Injury

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

The purpose of this study is to examine the usefulness of the Grief Recovery Method in assisting persons with spinal cord injuries to achieve as complete a recovery as possible, thereby allowing for fuller participation in life.

NCT ID: NCT01894802 Recruiting - Spinal Cord Injury Clinical Trials

Cortical Recording and Stimulating Array Brain-Machine Interface

CRS-BMI
Start date: December 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this research study is to demonstrate the safety and efficacy of using two CRS Arrays (microelectrodes) for long-term recording of brain motor cortex activity and microstimulation of brain sensory cortex.

NCT ID: NCT01889381 Recruiting - Facial Injuries Clinical Trials

Human Craniomaxillofacial Allotransplantation

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

Background: The human face is critically important for breathing, eating, seeing, and speaking/ communicating, but its most important job may be to look like a human face. Devastating facial deformities often cause affected individuals to avoid human contact and disappear from society. Although current surgical advancements can somewhat restore facial defects, this process often requires many operations and the resulting face only resembles the human face. To date, over 20 face transplants have been performed with highly encouraging functional and aesthetic results, but widespread clinical use has been limited due to the adverse effects of life-long and high-dose immunosuppression needed to prevent graft rejection. Risks include infection, cancer, and metabolic problems, all of which can greatly affect recipients' quality of life, make the procedure riskier, and jeopardize the potential benefits of face transplantation. Study Design: This non-randomized, Phase II clinical trial will document the use of a new immunomodulatory protocol (aka - Pittsburgh Protocol, Starzl Protocol) for establishing face transplantation as a safe and effective reconstructive treatment for devastating injuries/ defects by minimizing maintenance immunosuppression therapy in face transplant patients. This protocol combines lymphocyte depletion with donor bone marrow cell infusion and has enabled graft survival using low doses of a single immunosuppressive drug followed by weaning of treatment. Initially designed for living-related solid organ donation, this regimen has been adapted for use with grafts donated by deceased donors. The investigators propose to perform 15 full or partial human face transplants employing this novel protocol. Specific Aims: 1) To establish face transplantation as a safe and effective reconstructive strategy for the treatment of devastating facial injuries/defects; 2) To reduce the risk of rejection and enable allograft survival while minimizing the requirement for long-term, high-dose, multi-drug immunosuppression. Significance of Research: Face transplantation could help injured individuals recover functionality, self-esteem, and the ability to reintegrate into family and social life as "whole" individuals. This protocol offers the potential for minimizing the morbidity of maintenance immunosuppression, thereby beneficially shifting the risk/benefit ratio of this life-enhancing procedure and enabling a wider clinical application of face transplantation.

NCT ID: NCT01847742 Recruiting - Clinical trials for Psychological Trauma

EMDR Intervention for Psychological Trauma Among Syrian Refugees

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

To implement an EMDR (Eye Movement Desensitization and Reprocessing)intervention to treat the trauma symptoms among Syrian Refugees.

NCT ID: NCT01821690 Recruiting - Clinical trials for Traumatic Brain Injury

Buspirone for the Treatment of Traumatic Brain Injury (TBI) Irritability and Aggression

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

The purpose of this study is to improve behavior control displayed by persons with traumatic brain injury by assessing effectiveness of treatments for post-TBI irritability and aggression.

NCT ID: NCT01812941 Recruiting - Trauma Clinical Trials

Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients

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

The purpose of this project is to evaluate the level of mitochondrial dysfunction several patient populations: Burn, trauma, and control group of healthy volunteers. Study hypothesis: Increased plasma concentrations of a newly discovered inflammatory mediated, called mtDNA DAMPS associated with the occurrence of multi-organ dysfunction syndrome in severly injured patients. As the severity of a burn injury or trauma injury increase, so will systemic mitochondrial dysfunction.

NCT ID: NCT01760135 Recruiting - Trauma Clinical Trials

Nutritional Requirement for the Severe Trauma Patients

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

After severe trauma, high caloric nutrition supplement do harm on metabolic and immunologic aspects.