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Wounds and Injuries clinical trials

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NCT ID: NCT06153953 Not yet recruiting - Diabetic Wound Clinical Trials

A Comparative Study Between Vacuum Therapy Dressing and Conventional Dressing in Management of Diabetic Wounds

Start date: December 2023
Phase: N/A
Study type: Interventional

Diabetes is a global epidemic and a leading cause of death by disease. An estimated 366 million people worldwide had diabetes in 2011.(1).The incidence of diabetic foot ulcers (DFUs) and diabetic complications increases as the age increases.(2).Up to 25% of patients with diabetes will suffer from a foot ulcer during their lifetime. Ulceration is a pivotal factor in the causal pathway to infection and amputation.(3,4).Diabetic foot ulcers (DFUs) are the main cause of hospitalization in diabetic patients and they are considered a worldwide health problem. In recent years, the improvement in diabetes therapy and the reinforcement of guidelines have reduced the amputation rate.(5).The etiology of DFU is complex and rarely unifactorial. In general, foot ulcers are the cumulative result of repetitive trauma that wears a hole in the skin. The triad of neuropathy, foot deformity, and minor considers as the major contributing factors of ulcer development.(6).Vacuum therapy or Negative Pressure Wound Therapy is a technology uses a piece of foam in contact with the wound bed, covered by an occlusive dressing and placed under sub atmospheric pressure.(7).In other words NPWT is a non-invasive therapy system that uses controlled negative pressure using a vacuum device to promote wound healing by removing fluid from open wounds through a sealed dressing or a foam dressing connected to a collection container using sub-atmospheric pressure.(8).The system produces granular tissue that has a characteristic rough appearance. The device can decrease the depth and area of large diabetic foot wounds into a shallow, smaller wound.(8,9).NPWT was first proposed by Argenta and Morykwas in 1997. From then it has been approved as an effective modality of dressing in chronic wounds.(1).NPWT is a safe modality of dressing it has shown a few complications. Minor complications encountered in the vacuum-treated patients : erosion of adjacent tissue due to increased local pressure underneath the tubing ,mild reactions of the peri-wound area (i.e. maceration and eczema) , and sudden increase in body temperature.(10)

NCT ID: NCT06151327 Completed - Pressure Injury Clinical Trials

Alternating Pressure Air Mattress and Pressure Injury Prevalence

APAM
Start date: October 20, 2023
Phase:
Study type: Observational

explore the correlation of accurate implementation of APAM and pressure injury prevalence

NCT ID: NCT06150326 Not yet recruiting - Critical Illness Clinical Trials

Medical Honey for Wound Treatment in Intensive Care. (MICARéa) Randomized, Controlled, Single-center Pilot Study.

MICAREA
Start date: January 2024
Phase: Phase 2/Phase 3
Study type: Interventional

Wound management is a real public health issue in France. To date, a wide range of devices exists to treat these wounds, depending on their nature and stage of evolution. Honey has been proposed for the care of wounds and is effective in reducing the surface of wounds and the pain perceived by patients. Inanition, its use is very simple compared to usual care, requiring different types of dressing accross time. In the intensive care unit, patients are prone to suffering or developing numerous types of wound, but the interest of honey has not been investigated yet. We propose a prospective, monocentric, randomized, single-blind, controlled clinical trial to assess the efficacy of managing acute cutaneous wounds with honey (Activon®) compared with standard care, in intensive care patients. The primary endpoint is the percentage of wound surface area reduction measured at 15 days from inclusion.

NCT ID: NCT06150196 Recruiting - Clinical trials for Post-traumatic Stress Disorder

Brain Health & Wellness Classes for Veterans With Traumatic Brain Injury

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

This study is testing the usefulness of two types of Brain Health & Wellness classes for Veterans with a history of concussion to improve mental health.

NCT ID: NCT06149975 Not yet recruiting - Clinical trials for Traumatic Brain Injury

Feasibility of a Motor-cognitive Training Program in Patients With Traumatic Brain Injury

Start date: November 20, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical study is to test feasibility of a motor-cognitive training program in patients after mild to severe traumatic brain injury in an acute hospitalization setting. The intervention is a step-based dual-task training, i.e. patients are presented with step patterns that they have to memorize and then execute in the tempo given by a metronome. Researchers will assess the feasibility of the motor-cognitive training regarding acceptance and safety, user evaluation of the training and training performance.

NCT ID: NCT06148363 Recruiting - Clinical trials for Transcranial Direct Current Stimulation

Intervention Effect of High-Definition Transcranial Direct Current Stimulation (HD-tDCS) on Non-suicidal Self-injury (NSSI)

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

To investigate the intervention effect of high-definition transcranial Direct Current Stimulation (HD-tDCS) on patients with Non-suicidal Self-injury (NSSI) and its underlying neural mechanism by magnetic resonance imaging (MRI).

NCT ID: NCT06148324 Not yet recruiting - Clinical trials for Traumatic Brain Injury

MENTOR Wellness Program

Start date: January 2024
Phase: N/A
Study type: Interventional

This randomized trial aims to determine the effectiveness a virtual wellness intervention program in individuals with traumatic brain injury (TBI). Participants will be randomized at enrollment into two groups: immediate treatment (IT) and delayed treatment (DT) group. This study will also provide insights into the impact of these intervention's components in helping emotional, physical, and nutritional outcomes post-injury in the context of social determinants of health (SDOH).

NCT ID: NCT06147804 Not yet recruiting - Clinical trials for Urinary Bladder Trauma

Managment and Outcome of Urinary Bladder Trauma After Gynaecological and Obstetric Operations

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

We aimed to evaluate the management and outcome of bladder trauma after gynecological and obstetric operations at Assiut university hospital and to evaluate the methods of treatment of these complications. We aimed to find out risk factors for vesico uterine fistula after bladder trauma

NCT ID: NCT06147258 Not yet recruiting - Clinical trials for Spinal Cord Injuries

The Impact of Expressive Emotional Writing on Facilitating Grief Resolution in Adults With Spinal Cord Injury

Start date: January 8, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the therapeutic benefits of a 10-week online coach-guided EEWP on psychosocial health among adults with SCI.

NCT ID: NCT06146829 Not yet recruiting - Clinical trials for Postoperative Acute Kidney Injury

Machine Learning Models for Prediction of Acute Kidney Injury After Noncardiac Surgery

Start date: November 27, 2023
Phase:
Study type: Observational

Acute kidney injury (AKI) is a common surgical complication characterized by a rapid decline in renal function. Patients with AKI are at an increased risk of developing chronic kidney disease and end-stage renal disease, which has been associated with an increased risk of morbidity, mortality and financial burdens. Identifying high-risk patients for postoperative AKI early can facilitate the development of preventive and therapeutic management strategies, and prediction models can be helpful in this regard. The goal of this retrospective study is to develop prediction models for postoperative AKI in noncardiac surgery using machine learning algorithms, and to simplify the models by including only preoperative variables or only important predictors.