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Wounds and Injuries clinical trials

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NCT ID: NCT03225625 Enrolling by invitation - Clinical trials for Spinal Cord Injuries

Stem Cell Spinal Cord Injury Exoskeleton and Virtual Reality Treatment Study

SciExVR
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The SciExVR study will evaluate the potential benefit of autologous bone marrow derived stem cells (BMSC) in the treatment of spinal cord injury with evidence of impaired motor or sensory function. The treatment consists of bilateral paraspinal injections of the BMSC at the level of the injury as well as superior and inferior to that spinal segment followed by an intravenous injection and intranasal placement. Patients undergoing BMSC treatment may also be assigned to use of exoskeletal movement (or equivalent) or virtual reality visualization (or equivalent) to augment upper motor neuron firing and/or receptivity of the sensory neurons. http://mdstemcells.com/sciexvr/

NCT ID: NCT02769416 Enrolling by invitation - Clinical trials for Traumatic Brain Injury

The National Center for Testing Treatments in Chronic Spinal Cord and Traumatic Brain Injury

NCTT
Start date: December 2015
Phase:
Study type: Observational [Patient Registry]

The NCTT is a prospective, multicenter, observational research network for subjects with chronic spinal cord and/or chronic traumatic brain injury.

NCT ID: NCT02749760 Enrolling by invitation - Clinical trials for Upper Extremity Injuries

Prevention of Ulnar Collateral Ligament (UCL) Injuries in Minor League Pitchers

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

This is a study of the muscle stabilizers of the elbow with respect to the prevention of Ulnar Collateral Ligament (UCL) injuries in pitchers. Pitchers are assessed at spring training and end of season for approximately 5 years. Pronator, flexor digitoum superficialis (FDS), and wrist flexion strength will be measured and correlated with upper extremity injuries and time missed from pitching. The investigators will also be measuring loss of strength over the season. The goal is to learn whether strength in these muscles prevents UCL injuries and finally whether these muscles can be strengthened to avoid such injuries.

NCT ID: NCT02746978 Enrolling by invitation - Spinal Cord Injury Clinical Trials

A Patient-centered Approach to Successful Community Transition After Catastrophic Injury

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

Shepherd Center is bringing a more patient-centered focus to educational, peer-support, and technology resources offered to patients with spinal cord injury and their families and is evaluating these changes. Approximately 740 patients have provided information about healthcare utilization following inpatient rehabilitation. This information will help Shepherd Center staff follow utilization trends and plan programs targeted at the high-use areas.

NCT ID: NCT02688049 Enrolling by invitation - Spinal Cord Injury Clinical Trials

NeuroRegen Scaffold™ Combined With Stem Cells for Chronic Spinal Cord Injury Repair

Start date: January 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of mesenchymal stem cells or neural stem cells combined with NeuroRegen scaffold transplantation in patients with spinal cord injury.

NCT ID: NCT02682966 Enrolling by invitation - Clinical trials for Postoperative Myocardial Injury

Direct Evaluation of Postoperative Myocardial Injury Using Coronary Computed Tomography Angiography After Non-Cardiac Surgery

Start date: September 2016
Phase: N/A
Study type: Observational

This is a prospective study in patients who undergo routine postoperative troponin assessment after major (semi-)elective noncardiac surgery. Two groups are created based on postoperative troponin levels: Postoperative myocardial injury (PMI) group with troponin I levels ≥ 60 ng/L and a control group with troponin levels < 60ng/L. The primary aim of this study is to assess the association of PMI with pulmonary embolism. Additionally, the association between PMI and obstructive CAD will be investigated.

NCT ID: NCT02677285 Enrolling by invitation - Skin Graft Clinical Trials

Bioimpedance Based Monitoring of Operation Wound and Skin Graft Healing

Start date: January 2016
Phase:
Study type: Observational

This study consists of two clinical series. With the first series investigators monitor the healing of skin grafts with bioimpedance measurements. The bioimpedance measurement is done with a purpose built patch that has electrodes in contact with the wound and reference electrodes. In the second series the investigators monitor closed operational wounds (breast reconstruction surgery patients) with bioimpedance measurements. This series is also conducted with bioimpedance measurements but the wounds are operational wounds. Both groups will have 20 patients.

NCT ID: NCT02652598 Enrolling by invitation - Brain Injuries Clinical Trials

Evaluate the Effects of Tolcapone on Cognitive and Behavioral Dysfunction in Patients With BI and NCD

Start date: November 2015
Phase: Phase 2
Study type: Interventional

The experimental design is an open-label two-week trial of tolcapone to evaluate which clinical domains are affected by tolcapone treatment and to identify "responders" to tolcapone treatment in the two subject groups (BI and NCD)

NCT ID: NCT02623660 Enrolling by invitation - Wounds and Injuries Clinical Trials

Microcurrent Stimulation Reduces Post-Operative Swelling and Healing Time Following Knee Replacement Surgery

Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if patients undergoing a total knee arthroplasty (TKA) experience a clinically significant reduction in healing time when treated post operatively with a specific form of micro and nano-ampere current. The results of this trial will provide a basis for generalizing its outcomes to apply to other joint replacements and revisions by reducing edema and inflammation and therefore will result in a shorter time to heal. The study will compare electrically treated and non electrically treated patients by using digitally based measurements to determine objective reductions of lower extremity edema including intra and inter cellular shifts in fluid distribution, increased range of motion (ROM) and muscle strength, and improved functional tests of ambulation.

NCT ID: NCT02602639 Enrolling by invitation - Spinal Cord Injury Clinical Trials

Functional Electrical Stimulation With Rowing as Exercise After Spinal Cord Injury

FES
Start date: October 2015
Phase: N/A
Study type: Interventional

Currently, those with spinal cord injury (SCI) demonstrate increased prevalence of obesity (75%) cardiovascular disease (30 - 50%), type II diabetes (21%) and osteoporosis in the legs (100%) when compared to the general population. It is important to identify the modes and intensities of exercise most likely to generate a reduction in these inactivity-related diseases in this population. Therefore, the main purpose of this pilot research project is to implement and test a form of a spinal cord injury-specific exercise, known as FES rowing (FES: functional electrical stimulation).