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Wounds and Injuries clinical trials

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NCT ID: NCT02836990 Completed - Wound Infection Clinical Trials

Prevena™ vs Dermabond in Groin Wound Infections in Vascular Surgery

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

This study evaluates the clinical efficacy and cost effectiveness of Prevena Incision Management System versus Dermabond in preventing groin wound infections in patients who undergo vascular surgery requiring a groin wound. Half of the patients will receive Dermabond and the other half will receive the Prevena Incision Management System for their groin wounds.

NCT ID: NCT02836951 Completed - Clinical trials for Traumatic Brain Injury

Rapid Diagnostics for Traumatic Brain Injury (TBI)

Start date: September 2016
Phase:
Study type: Observational

Novel biomarkers of traumatic brain injury (TBI) have been discovered in laboratory animal models. The objective of this study is to find whether similar markers are detectable in the body fluids of human subjects that have sustained a TBI.

NCT ID: NCT02831907 Completed - Acute Kidney Injury Clinical Trials

Portal Flow Pulsatility as a Risk Factor for Acute Kidney Injury After Cardiac Surgery

PP-AKI
Start date: August 2016
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the possible association between portal vein flow pulsatility and acute kidney injury after cardiac surgery. Participants will undergo assessment of portal vein flow and intra-renal blood flow using bedside Doppler ultrasound before surgery and daily for three days after cardiac surgery.

NCT ID: NCT02831166 Completed - Clinical trials for Myocardial Infarction

Vascular Closure Device Versus Transradial Approach in Primary Percutaneous Coronary Intervention

ARISE-2
Start date: January 2016
Phase: Phase 4
Study type: Interventional

Primary percutaneous coronary intervention represents the gold standard for the treatment of ST-segment-elevation acute myocardial infarction. However, periprocedural bleedings are associated with an increased risk of mortality, re-infarction, and stroke. Although the prognostic value of access site related bleeding complications is still debated, transradial approach is associated with better short-term outcomes and reduced hospital stay as compared to transfemoral approach. The investigators aimed to compare transradial approach with transfemoral approach with systematic achievement of hemostasis by the implantation of a vascular closure device in a national multicentre randomized clinical trial.

NCT ID: NCT02831062 Completed - Clinical trials for Chronic Kidney Disease

Nutritional Therapy to Prevent Progression of Acute Kidney Injury to Chronic Kidney Disease

NutriAKI
Start date: August 1, 2016
Phase: N/A
Study type: Interventional

This study will evaluate patients who have an episode of moderate to severe acute kidney injury (AKI) and are followed in a focused post-AKI clinic. After patients present signs of kidney recovery and before hospital discharge, patients who give consent will be enrolled in the study. At the first post-AKI clinic visit, patients will be randomly allocated to follow a normal (ad-lib) or a low protein diet (LPD) for 3 months. Patients allocated to a LPD will receive a drug called Ketosteril. This drug allows the intake of essential amino acids while minimizing the amino-nitrogen intake, what in excess, can be bad for the recovered kidney. The investigators will evaluate the nutritional parameters and the kidney recovery of all patients and compare these parameters in those two groups.

NCT ID: NCT02830035 Completed - Wounds and Injuries Clinical Trials

Real-Time Ultrasound-guidance Facilitates Paramedian Spinal Anaesthesia

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

The purpose of this study is to compare the clinical efficacy of real-time ultrasound guidance on spinal anesthesia vs the traditional anatomical landmark technique, by comparing success rate of spinal needle insertion, success rate rate of single needle pass, duration and immediate complications.

NCT ID: NCT02828527 Completed - Mild Head Injury Clinical Trials

Care Courses for Mild Head Injury Patients

Start date: September 12, 2014
Phase: N/A
Study type: Observational

Background / Rationale at. The mild head injury. In France, the incidence of head injuries is estimated at 100,000 per year in France. 80% of mild head trauma. This is a pattern of frequent use of the health system. The reason for consultation, benign appearance, present a significant risk of complication. In 15 to 25% of the evolution of head injury is unfavorable. Disorders of attention, memory disorders, psychiatric events and mood changes may occur. These symptoms are grouped into a syndrome, post-concussion syndrome. The post-concussion syndrome: It affects approximately 20,000 people per year in France. This is a common disease and most undervalued in the general population. diagnostic criteria post-concussional disorder according to DSM-IV (Diagnostic and Statistical Manual). Symptoms may persist for more than 3 months after head injury. This syndrome is responsible for suffering, personal and professional sound and quality of life of patients. It is particularly debilitating in everyday life, and can have disastrous consequences on their family, social, cultural and professional. It gives rise to many financial implications with compensation requirements and expertise consultations. Intention of work In a recent study by a team of neuropsychologists Kremlin Bicetre, it has been shown that screening and early treatment of post-concussion syndrome from the slight head injury prevents chronicity of symptoms.

NCT ID: NCT02827448 Completed - Heart Failure Clinical Trials

Effectiveness of NephroCheckTM Test to Predict Acute Kidney Injury Following Advanced Cardiac Replacement Therapies

Start date: November 2015
Phase:
Study type: Observational

The purpose of this study is to test how well the NephroCheckTM Test, a noninvasive laboratory test performed on urine, predicts loss of kidney function in patients that have had a heart transplant or a Left Ventricular Assist Device (LVAD) or Total Artificial Heart (TAH) implanted.

NCT ID: NCT02820350 Completed - Acute Kidney Injury Clinical Trials

Safety and Efficacy of a Selective Cytopheretic Device (SCD) in Pediatric Patients With Acute Kidney Injury (AKI).

SCD-PED-01
Start date: December 4, 2016
Phase: N/A
Study type: Interventional

The SCD (Selective Cytopheretic Device) is an extracorporeal device used as an adjunct to renal replacement therapy (RRT) to improve the outcomes of pediatric patients with acute kidney injury (AKI). Funding Source - FDA OOPD (SCD-PED-01)

NCT ID: NCT02807584 Completed - Burns Clinical Trials

Treatment of Wounds With a New Adhesive Foam Dressing

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

This study will look at whether ELECT, a new adhesive foam dressing, can offer an alternative to traditional wound care methods. Patients will be treated with ELECT for 14 days. Data relating to wound healing, the performance of the dressing and the opinion of the doctor will be collected. The hypothesis of this study is that the ELECT foam adhesive dressing is 'fit for purpose' and will be effective at treating a variety of wounds.