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Wounds and Injuries clinical trials

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NCT ID: NCT03899532 Recruiting - Clinical trials for Traumatic Brain Injury

Remote Ischemic Conditioning in Traumatic Brain Injury

MOTION
Start date: September 24, 2019
Phase: N/A
Study type: Interventional

Traumatic brain injury (TBI) is a leading cause of death among trauma patients accounting for one-third of all trauma mortalities. Patients who survive the initial trauma are liable to secondary insults from the ensuing inflammatory state in the brain. Treatment goals are aimed at reducing secondary injury. Maintaining adequate brain perfusion, limiting cerebral edema, and optimizing oxygen delivery are part of established treatment protocols. Numerous therapeutics have been evaluated as potential treatment for TBI with very limited success and there is no medication that alters survival. Various novel therapeutic options have been investigated to prevent the secondary brain injury. Remote Ischemic Conditioning (RIC) is one of these therapies. RIC involves decreasing blood flow to a normal tissue usually the arm by inflating the blood pressure cuff 30mmHg over the systolic blood pressure. The decreased blood flow or ischemia is maintained for 5 minutes followed by releasing the pressure and re-perfusion of the arm. This cycle is usually repeated 4 times. RIC has been shown to improve outcomes in patients with heart attacks, strokes, elective neurosurgeries. A prospective observational study and a randomized clinical trial has shown the protective effect of RIC in TBI patients. Additionally, multiple studies in animals have shown that RIC is neuroprotective after TBI. RIC is non-invasive and harmless except for a little discomfort in the arm. The aim of the study is to evaluate the impact of RIC on long term outcomes in patients with TBI.

NCT ID: NCT03897335 Recruiting - Acute Kidney Injury Clinical Trials

Preventing Acute Kidney Injury (AKI) in Pediatric Patients

AKI
Start date: February 7, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effects of peri-operative administration of Aminophylline versus Saline placebo in the preservation of renal function and the attenuation of renal injury in pediatric patients undergoing open heart surgery.

NCT ID: NCT03894267 Recruiting - Wounds Clinical Trials

An Evaluation of the Impact of a Wound Dressing on Pressure Ulcer Incidence.

Start date: March 12, 2019
Phase: N/A
Study type: Interventional

A pressure ulcer (PU) is localized injury to the skin and/or underlying tissue usually over a bony prominence, as a result of pressure, or pressure in combination with shear. PUs are common, affecting up to 40% of participants receiving health care. Furthermore, PUs impact negatively on an individual's health related quality of life, with pain being the most frequently cited complaint. PUs commonly occur in those who cannot reposition themselves to relieve pressure/shear over bony prominences. The ability to reposition is often diminished in the very old, the malnourished and those with acute illness. Pressure ulcers are common devastating wounds, extending from deep in the bone and muscle layers through to the skin, occurring most often in older persons with limited mobility. They contribute to significant morbidity and mortality as they are smelly, highly painful and very prone to infection. Existing research carried out by the RCSI School of Nursing and Midwifery shows that both high and low movers are at risk of pressure ulcer development.

NCT ID: NCT03882983 Recruiting - Chronic Wounds Clinical Trials

Stromal Vascular Fraction From Lipoaspirate to Treatment of Chronic Non-healing Wound

Start date: September 1, 2017
Phase: Phase 1
Study type: Interventional

This is a Phase I, open-label, single arm study to demonstrate the safety of Antria Cell Preparation Process during fat grafting augmented with autologous adipose derived stromal vascular fraction to demonstrate the safety and efficacy of administration of SVF enriched fat grafting in chronic wounds

NCT ID: NCT03882502 Recruiting - Aphasia Clinical Trials

Electrical Stimulation in Traumatic Brain Injury (TBI) Induced Aphasia

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to investigate whether a tDCS-accompanied intensive naming therapy leads to a performance improvement in patients with chronic aphasia induced by a moderate TBI

NCT ID: NCT03880110 Recruiting - Acute Kidney Injury Clinical Trials

Early Prediction of Acute Kidney Injury in High Risk Patients After Non-cardiac Surgery

Start date: May 20, 2019
Phase:
Study type: Observational

Acute kidney injury (AKI) is a common complication after non-cardiac surgery with adverse short and long term morbidity and mortality. So far there have been no effective therapy for AKI treatment developed, possibly due to the heterogenicity of this syndrome. Therefore, prevention of AKI in high risk patients undergoing non-cardiac surgery, as emphasized by Kidney Disease Improving Global Outcomes (KDIGO), becomes the first priority. However, early prediction of AKI is the first step before taking preventive measures, which really make a great challenge to clinical practitioners because of such a limited time window and complex clinical scenarios. Recently, cumulative evidence have shown that biomarkers and renal ultrasound may play an important role in AKI prediction after non-cardiac surgery. The purpose of this study is to investigate the combination of biomarkers, urine sedimentation and renal resistive index for early prediction of AKI in high risk patients undergoing non-cardiac surgery.

NCT ID: NCT03877081 Recruiting - Sepsis Clinical Trials

Effect of Probiotics and Prebiotics in Renal Function in Septic Acute Kidney Injury Patients

Start date: January 4, 2019
Phase: Phase 3
Study type: Interventional

Septic acute kidney injury is a condition associated with highly related to inflammatory molecules. Prebiotics and probiotics have shown to improve inflammatory cascade in animal model; In this study, the investigators propose the use of probiotics to improve the clinical evolution of septic acute kidney injury patients.

NCT ID: NCT03874416 Recruiting - Clinical trials for Moderate to Severe Traumatic Brain Injury

Cognitive Rehabilitation of Working Memory After Moderate to Severe Traumatic Brain Injury

REHAB-MDT
Start date: January 25, 2021
Phase: N/A
Study type: Interventional

The study aims to demonstrate improvement of daily life functioning and improvement of cognitive tests in post traumatic brain injury (TBI) patients suffering from working memory deficit, by a 3-month specific cognitive rehabilitation program, in comparison with patients with usual non-specific rehabilitation of same duration. As secondary objectives, the study aims to: - demonstrate improvement of specific neuropsychological tests of working memory; - demonstrate improvement of non-specific tasks involving working memory; - assess the evolution in not-targeted domains by the specific rehabilitation, which would give evidence of a global cognitive stimulation effect; - demonstrate improvement of social integration ability and quality of life; - demonstrate persistence of effects at 3 months and 6 months after the end of treatment; - demonstrate the acceptability, the tolerance and the feasibility of rehabilitation.

NCT ID: NCT03874247 Recruiting - Clinical trials for Acute Traumatic Injury

Clinical Trial to Evaluate the Efficacy and Safety of 'Pelubiprofen Controlled Released Tab.' in Acute Traumatic Injury

Start date: February 25, 2019
Phase: Phase 3
Study type: Interventional

A randomized, double-blind, placebo-controlled, parallel, multi-center phase III clinical trial

NCT ID: NCT03874208 Recruiting - Clinical trials for Traumatic Brain Injury (TBI)

Prediction for Coma Recovery With Comaweb

COMASCORE
Start date: January 15, 2020
Phase: N/A
Study type: Interventional

The general objective of the comaScore project is to provide an external validation of the accuracy of the comaScore, a score derived from magnetic resonance imaging (MRI), to predict 1 year outcome of patients unresponsive to simple orders after traumatic brain injury (TBI), aneurysmal subarachnoid hemorrhages (aSAH) and cardiac arrest (CA) in the day 7 - day 45 period post brain injury.