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Active clinical trials for "Wounds and Injuries"

Results 1691-1700 of 4748

Topical Silver for Prevention of Wound Infection After Cesarean Delivery

Wound Infection

A common concern in any surgical procedure is the occurrence of infection. Silver-containing treatments are popular and used in wound treatment; however, there is presently little evidence of the effectiveness of silver-containing treatment for the prevention of obstetrical wound infection. We plan to investigate the rate of infection in women experiencing cesarean sections at Vanderbilt University Medical Center (VUMC) by comparing the infection rate based on a randomized choice of silver-containing wound dressings to soft cloth adhesive wound dressings.

Terminated4 enrollment criteria

Neural Bases of Cognitive Rehabilitation for Brain Injury

Brain Injury

Some of the most common and disabling consequences of brain injury are deficits in cognition, such as difficulty with sustained attention, memory, organization, and goal management. The long-term goal of this research program is to develop and test novel neuroscience-based cognitive interventions for improving attentional regulation and related "executive function" brain processes involved in goal-directed behavior.

Completed10 enrollment criteria

Effectiveness of Automated Locomotor Training in Patients With Acute Incomplete Spinal Cord Injury:...

Spinal Cord Injuries

The purpose of this study is to determine whether longer locomotor training results in a mor favorable outcome in patients with incomplete spinal cord injury.

Completed13 enrollment criteria

Lithium, Cord Blood Cells and the Combination in the Treatment of Acute & Sub-acute Spinal Cord...

Spinal Cord Injury

The trial is to investigate the safety and efficacy of oral lithium, intraspinal umbilical cord blood mononuclear cell transplant, and the combination in the treatment of acute and subacute spinal cord injury

Completed17 enrollment criteria

Ciclosporin to Reduce Reperfusion Injury in Primary PCI

Myocardial Reperfusion Injury

Routine primary percutaneous coronary intervention (PPCI) for a heart attack involves opening a blocked artery with a balloon then inserting a metal scaffold (stent) to hold the artery open. During this procedure inflammation can occur causing further damage to the heart. The objective of this trial is to determine whether administration of the drug ciclosporin prior to PPCI reduces the amount of damage to the heart relative to treatment with placebo. The damage to the heart is assessed after 12 weeks by an magnetic resonance imaging (MRI) scan. Patients are followed-up after 12 months participation in the study. This is a single centre study looking to recruit 68 patients.

Completed25 enrollment criteria

Study to Evaluate Clinical Efficacy and Safety of "Medifoam H" in Wound Healing

Trauma

The wound healing efficacy and safety of "Medifoam H" in patients with minor, acute trauma. The hypothesis of this study is that using "Medifoam H" dressing for a week is not inferior to using "Duoderm THIN" dressing in wound healing.

Completed9 enrollment criteria

Neuropathic Pain Study With Botulinum Toxin A in Spinal Cord Injury Patients

Spinal Cord InjuryNeuropathic Pain

The purpose of this study is to determine whether botulinum toxin A is effective in the treatment of neuropathic pain in spinal cord injury patients.

Completed10 enrollment criteria

Efficacy and Safety of Activated Recombinant Human Factor VII in Severely Injured Trauma Patients...

Acquired Bleeding DisorderTrauma

This trial is conducted in Africa, Asia, Europe, Oceania and North America. The aim of this trial is to evaluate the efficacy of activated recombinant human factor VII given in conjunction with standard therapy in the treatment of massive bleeding in subjects with severe blunt and/or penetrating trauma injury.

Completed10 enrollment criteria

Bowel Care and Cardiovascular Function After Spinal Cord Injury

Spinal Cord Injury

The main goal of this project is to determine the effects of lidocaine lubricant on cardiovascular function during routine bowel care in individuals with spinal cord injury. Bowel care is a common trigger of blood pressure and heart rate changes after spinal cord injury. In this project, we will be measuring blood pressure and heart rate non-invasively during normal bowel routine (which can be performed in the subject's home or at one of the investigators facilities). The measurements will occur twice over a period of 28 days: once using lidocaine lubricant and once using normal (placebo) lubricant. The recording equipment will be attached and subjects will have complete privacy during their bowel routine. The trial will be double-blind, meaning that neither the subject or the Nurse Continence Advisor who assists with testing will know which lubricant is being used for each test. The use of a lubricant gel containing an anesthetic is the standard of care in many hospital facilities when performing bowel care for individuals with spinal cord injury; however, it is not often used in the home setting. It is thought that using anaesthetic might reduce the cardiovascular effects of bowel care after spinal cord injury. However, it is not known whether this is the case. The investigators hypothesize that the lidocaine lubricant will alleviate some of the blood pressure and heart rate changes that occur during bowel care.

Completed12 enrollment criteria

Treatment of Severe Adult Traumatic Brain Injury Using Bone Marrow Mononuclear Cells

Traumatic Brain Injury

The purpose of this study is to determine if bone marrow harvest, BMMNC separation, and re-infusion in adults with acute severe TBI is safe and will improve functional outcome. 12/09/2015 Update: The study is closed to new enrollment and all follow-up visits have been completed. Data analysis is underway.

Completed30 enrollment criteria
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