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Wounds and Injuries clinical trials

View clinical trials related to Wounds and Injuries.

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NCT ID: NCT04804982 Completed - Acoustic Trauma Clinical Trials

Study of the Use of Hearing Protection Equipment in the Occurence of Acute Acoustic Trauma in the Army

QPROTEC
Start date: March 30, 2021
Phase:
Study type: Observational

Each year, military epidemiological surveillance counts approximately 1,000 acute acoustic injuries. Most are caused by exposure to weapon noise during training sessions while military personnel are provided with hearing protection. Several hypotheses could explain the occurrence of acute acoustic trauma despite wearing protections: - A lack of practices or knowledge about the use of hearing protection equipment that could facilitate the occurrence of acute acoustic trauma (improper fitting, use of an inappropriate type of protection, dropping of protectors, inappropriate removal) - A failure to seal the external ear canal due to an inappropriate plug size. These hypotheses will be explored using a questionnaire distributed to a population of Army soldiers training to shoot. The main objective is to determine the predictive factors corresponding to practices or knowledge related to the use of hearing protection equipment in the occurrence of acute acoustic trauma in a population of Army soldiers.

NCT ID: NCT04800757 Completed - Work-related Injury Clinical Trials

VALES+Tú: Targeting Psychosocial Stressors to Reduce Latino Day Laborers (LDL) Injury Disparities

Start date: May 11, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of VALES+Tú in reducing hazardous exposures at work and to determine the mediating effect of psychosocial stressors on VALES+Tú primary outcomes

NCT ID: NCT04798859 Completed - Rehabilitation Clinical Trials

The Child in Context Intervention Study

CICI
Start date: May 10, 2021
Phase: N/A
Study type: Interventional

Children with acquired brain injury (ABI) often struggle with complex impairments, including cognitive (such as memory and attention), social, emotional and behavioral challenges. There is a lack of evidence-based knowledge about rehabilitation for children with ABI in the chronic phase. The current study, the CICI Study, is a randomized controlled trial (RCT) directed towards children with ABI and their families in the chronic phase. The study will be conducted in close collaboration with schools and local health care providers. The CICI Study focuses on the child's and parents' individually identified target outcome areas and rehabilitation goals. The intervention aims to enhance everyday functioning in the home and school environment by attaining rehabilitation goals in areas noted as challenging by the participants. The efficacy of the CICI-intervention will be measured in terms of goal attainment, burden of brain injury related symptoms, parenting self-efficacy, unmet health care needs, as well as several aspects of child, parent and family functioning.

NCT ID: NCT04796753 Completed - Clinical trials for Musculoskeletal Injury

Detection of Neuromuscular Deficits in Uninjured Youth Basketball Players

DPL
Start date: October 1, 2018
Phase:
Study type: Observational

Basketball is an impact, coordination-opposition sport with continuous contact among players and it is considered a sport of medium-high injury incidence. Players are force to have a physical condition appropriate to their practice and the demand to which they must respond due to the intensity of the efforts this sport requires. In order to achieve this, it is necessary to establish an evaluation protocol that allows the detection of functional deficiencies, to guide and conduct in a specific and early way every moment of players' health and growth. The purpose of this study is to evaluate and detect federated youth basketball players' (U12 - U17) neuromuscular deficiencies in mobility, stability and landing technique in static and dynamic situations to simulate all the most important actions of basketball demands.

NCT ID: NCT04796298 Completed - Clinical trials for Sports Physical Therapy

Interventions and Viscoelasticity of Hamstring

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

The study aims to investigate acute effects of ballistic hamstring stretching, hamstring extender exercise, and kinesiotaping application on viscoelasticity of hamstrings and standing long jump performance on rowers.

NCT ID: NCT04794881 Completed - Meningitis Clinical Trials

Repeat Lumbar Puncture at 24 Versus 48 Hours After Traumatic Lumbar Puncture in Neonates

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

Visibly traumatic as well as microtraumatic lumbar punctures (LP) are very common in the neonatal period. The presence of blood makes it difficult to interpret cerebro-spinal fluid (CSF) findings. Clinicians often perform a repeat LP in the hope that some of the red blood cells would have cleared by then, allowing a better interpretation of the CSF findings. There is no published information whether a repeat LP provides any added information to the original traumatic LP, and if so what is the best time to repeat an LP after a traumatic LP. In this randomised controlled trial (RCT), we plan to randomly allocate neonates following a visibly traumatic LP to either undergo a repeat LP at 24 hours or 48 hours later to determine which LP gives more accurate results.

NCT ID: NCT04794621 Completed - Wound Heal Clinical Trials

Electroceutical Dressing Technology (EDT) Against Wound Microbial Biofilm Infection

EDT BioFilm
Start date: June 3, 2021
Phase: N/A
Study type: Interventional

There are currently limited treatments available that show anti-biofilm efficacy for wound infection management Biofilms account for over 80% of infections and approximately 65% of nosocomial infections caused by microorganisms in the developed world involve biofilms. There clearly is a need for cost effective, highly stable, easily obtained biofilm targeted strategies for treatment of chronic wound biofilm infections. The information generated from this project has the potential of providing considerable benefits to wound care by determining the efficacy of EDT dressing in managing wound biofilm infection and efficacy in wound healing and closure. Such knowledge could help therapeutic strategies and could provide information for future clinical studies to further understanding -of EDT wound dressings.

NCT ID: NCT04794062 Completed - COVID-19 Clinical Trials

Myocardial Injury and Quality of Life After COVID-19

Start date: September 16, 2020
Phase:
Study type: Observational

In this observational study follow-up and dynamic observation will be conducted on the participants recovered from pneumonia caused by COVID-19. The main goal is an early diagnosis and detection of myocardial (heart) injury and quality of life in participants recovered from COVID-19 and follow-up in selected participants with present signs of myocarditis and/or myocardial fibrosis.

NCT ID: NCT04793490 Completed - Clinical trials for Post-Dural Puncture Headache

Sphenopalatine Ganglion Block for Management of Post- Dural Puncture Headache in Obstetric Patients

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this trial is to study the efficacy and efficiency of sphenopalatine ganglion block for management of post dural puncture headache in obstetric patients

NCT ID: NCT04785404 Completed - Wound Infection Clinical Trials

Primary Versus Secondary Closure of Stoma-Reversal Skin Wound

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

to compare infection rate stoma reversal skin wound after primary or secondary closure