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Wounds and Injuries clinical trials

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NCT ID: NCT02565121 Completed - Brain Injuries Clinical Trials

Olfaction Disorders in Patients Included in The Trauma Brain Injury (TBI) Database at Trondheim University Hospital

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

The aim of the study is to see whether patients with chronic smell impairment after brain injury benefit from a treatment that consists of corticosteroids, and then olfactory training in 3 months.

NCT ID: NCT02565043 Completed - Clinical trials for Surgical Wound Dehiscence

The Clinical Efficacy of RENASYS TOUCH NPWT System in the Management of Acute, Sub-acute and Chronic Wounds

NPWT
Start date: April 2015
Phase: N/A
Study type: Interventional

The study is looking at the clinical efficacy, functionality and device performance of a new Negative Pressure Wound Therapy (NPWT) system in the management of a variety of wound types, in a real-life clinical setting. The study will comprise a prospective, open-labeled, multi-center study in a number of care-settings (both hospital and community) in South Africa. The patient's reference wound will be randomized to treatment with either intermittent or continuous NPWT mode to assess whether the delivery of NPWT via each of these therapy settings will have an effect on the rate and quality of wound healing.

NCT ID: NCT02562001 Completed - Clinical trials for Spinal Cord Injuries

Association Between tDCS and Lokomat Training in Patients With Incomplete Spinal Cord Injury

Start date: May 6, 2015
Phase: N/A
Study type: Interventional

The spinal cord injury is identified as the major cause of permanent disability worldwide, with the loss of ability to walk being the largest and most devastating of them for these patients. Our goal is to analyze the effects of electrical transcranial direct-current stimulation (tDCS) combined with gait training with partial body weight support aided by robotic device (Lokomat, Hocoma) in the gait of patients with incomplete spinal cord injury (SCI). In this stratified randomized double-blind study, the participants will be randomly allocated into one of both groups, outpatients (GA) or inpatients (GI), and will receive active or placebo tDCS followed by gait training with Lokomat (GA: 3 sessions/week x 10 weeks = 30 sessions; GI: 5 sessions/week x 6 weeks = 30 sessions). The functional assessments (through clinical and functional scales, assess gait, muscle strength, spasticity, balance and pain) and neurophysiological (cortical excitability measured by transcranial magnetic stimulation, electroencephalography and functional near-infrared spectroscopy) will be held before and after the training period. The functional assessments will be also held after 15 sessions (intermediate) and after 3 months follow up. The expected result is that patients that received the active tDCS presents an improvement over the ground gait after the Lokomat training period significantly greater than the placebo group, with relations between neurophysiologic, kinematics and functional measurements.

NCT ID: NCT02561403 Completed - Clinical trials for TBI (Traumatic Brain Injury)

Brain Aging in Veterans (BRAVE) Training: A Cognitive Training Pilot Trial in Older Veterans With Traumatic Brain Injury

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

The purpose of this study is to conduct a pilot trial investigating cognitive training in older Veterans with a history of traumatic brain injury (TBI) to assess training effects, acceptability of training to participants, and to explore whether other factors influence training effects.

NCT ID: NCT02560675 Completed - Clinical trials for Chronic Pain Due to Injury

Why Does Acute Post Whiplash Injury Pain Transform Into Chronic Pain?

Start date: January 2016
Phase:
Study type: Observational

Why does acute post whiplash injury pain transform into chronic pain? Multi-modal assessment of risk factors and predictors of pain chronification

NCT ID: NCT02560480 Completed - Groin Injury Clinical Trials

Groin Injuries in Finnish Contact Sports

Finngroin
Start date: August 2015
Phase:
Study type: Observational

The prevalence of acute and chronic groin injuries in athletes is between 5 and 10 %. This observational case-control study follows three contact sport teams (soccer, ice-hockey and bandy) for two years to find out the prevalence and reasons for groin pain. Clinical examination, pain scores and pelvic magnetic resonance imaging (MRI) are performed. Hip and groin questionnaire (HAGOS) is used to determine severity of groin injuries.

NCT ID: NCT02556177 Completed - Clinical trials for Traumatic Brain Injury

Advanced MRI Applications for Mild Traumatic Brain Injury-Phase 2

mTBI-phase2
Start date: November 2015
Phase: N/A
Study type: Interventional

This is an open-label, non-randomized, prospective, multi-site, parallel group (segment), hypothesis-generating study designed to collect data that will aid in future scientific and engineering exploration of correlations between clinical neuropsychological assessments and GE Research Pack II advanced MR imaging in mTBI patients. The results are primarily intended for scientific inquiry and engineering development purposes, and may be used in future regulatory submissions.

NCT ID: NCT02554058 Completed - Spinal Cord Injury Clinical Trials

Combined Tactile and Proprioception Training After Spinal Cord Injury

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

A novel rehabilitation bike has been developed for patients with incomplete spinal cord injuries that incorporates mechanical stimulators on the bike pedals to stimulate the sensory receptors in the soles of the feet; the effect of mechanical stimulator on muscle strengthening has been reported by NASA to improve muscle atrophy in astronauts in zero-gravity environments. Cycling also stimulates lower limb position sensors. We predict that the combination of mechanical stimulation with cycling may be similar enough to walking over ground to lead to gains in balance and mobility. The present study will evaluate the therapeutic effect of this bike on balance, walking, as well as cortical-spinal and spinal pathways in patients with incomplete spinal cord injuries.

NCT ID: NCT02551510 Completed - Clinical trials for Wound Closure After Port Catheter Implantation

Comparison of Skin Adhesive to Subcuticular Suture Wound Closure After Port Placement

PWC
Start date: August 2015
Phase: N/A
Study type: Interventional

Port Wound Closure compares synthetic tissue adhesives with seam for cutaneous wound closure to port plant in terms of cosmetic results and time savings at comparable risk for wound infection.

NCT ID: NCT02547077 Completed - Clinical trials for Wound Closure Techniques

Use of 2-octylcyanoacrylate (Dermabond) Versus 5-0 Fast Absorbing Gut During Cutaneous Wound Closure

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

The purpose of this study is to determine whether the use of 2-octylcyanoacrylate during repair of linear cutaneous surgery wounds improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut.