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Wounds and Injuries clinical trials

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NCT ID: NCT05114057 Not yet recruiting - Acute Kidney Injury Clinical Trials

Use of NGAL for Fluid Dosing and CRRT Initiation in Pediatric and Neonatal AKI

Taking Focus 2
Start date: September 1, 2024
Phase: N/A
Study type: Interventional

This study will follow patients admitted to the PICU with sepsis, NICU with sepsis or after abdominal surgery, or CICU who are identified as being at risk for developing acute kidney injury. The investigators will use risk-stratification, biomarker testing, and a functional assessment to predict children and neonates who will become fluid overloaded and develop severe acute kidney injury.

NCT ID: NCT05111925 Recruiting - Clinical trials for Musculoskeletal Injuries

Pre- and Post-neuromusculoskeletal Injury Risk Evaluation for Return-to-Duty Enhancement

PREPARE
Start date: October 26, 2022
Phase:
Study type: Observational

The purpose of this study is to develop comprehensive and efficient pre- and post- musculoskeletal injury (MSKI) risk assessments for Service members, incorporating both objective and subjective measures. This is a multi-site observational study to identify the pre- and post-MSKI physical and psychosocial factors contributing to MSKI risks and undesired patient outcomes following MSKI. The study hypothesis is that a set of field-expedient clinical assessments can identify Service member specific MSKI risk factors and post-MSKI deficits that contribute to undesired patient outcomes and provide data to guide patient-specific risk mitigation and rehabilitation programs.

NCT ID: NCT05111587 Completed - Sport Injury Clinical Trials

Epidemiology of Injuries Caused by the Practice of Artificial Structure Climbing

EPITRAUMABLOC
Start date: November 16, 2021
Phase:
Study type: Observational

This study aims to precisely describe epidemiology of injuries than occur during practice of climbing in artificial structure. Each participant will complete questionnaires in order to identify injuries. The first questionnaire will be completed at the moment of the inclusion and the second questionnaire will be completed if participant has injuries every 3 months until month 12.

NCT ID: NCT05111535 Completed - Acute Kidney Injury Clinical Trials

Stockholm Acute Kidney Injury Cohort

SAKIS
Start date: January 1, 2009
Phase:
Study type: Observational

Since 2009, adult patients with acute kindney injury (AKI) at the department of Nephrology, Danderyd University Hospital and Karolinska Institutet, have been included in a prospective cohort. All patients were treated and evaluated according to a detailed clinical memorandum, and data collected prospectively. By 2020, 1861 patiens have been included of which 1519 fulfill current AKI criteria (as defined by KDIGO AKI guidelines) and will be evaluated regarding the following main research questions: 1. Descriptive study on patient characteristics, changes in biomarkers and in-hospital outcome. 2. One year outcome with focus on renal and cardiovascular outcomes. 3. Long-term outcome (up to 10 years) with focus on renal and cardiovascular outcomes.

NCT ID: NCT05111457 Completed - Injury;Sports Clinical Trials

Injuries in Swedish Padel

Start date: November 1, 2021
Phase:
Study type: Observational

The purpose of this project is to investigate the injury panorama of acute and overuse injuries in women and men who regularly participate padel. The intention is to provide insights on injury prevalence, injury location, injury consequences, gender differences and risk factors . This study will be conducted as a retrospective cohort study where the participants consist of female and male padle players, both at the recreational and competition level, with at least 6 months' experience in the sport. The information from this project can be valuable in the work of identifying risk factors for padle injuries and injury prevention strategies.

NCT ID: NCT05111093 Recruiting - Clinical trials for Spinal Cord Injuries

Epidural Electrical Stimulation to Restore Hemodynamic Stability and Trunk Control in People With Spinal Cord Injury

HemON
Start date: November 29, 2021
Phase: N/A
Study type: Interventional

The HemON study aims to evaluate the safety and preliminary efficacy of ARC-IM Therapy (Epidural Electrical Stimulation) to improve hemodynamic management and trunk control in people with sub-acute or chronic spinal cord injury (>= 1 month post injury) between C3 and T6 inclusive, who suffer from orthostatic hypotension.

NCT ID: NCT05110729 Recruiting - Quality of Life Clinical Trials

Quality of Life and Life Satisfaction in Pediatric and Adolescent Gymnasts Through Injury

Start date: November 12, 2021
Phase:
Study type: Observational

This study aims to assess the quality and life and life satisfaction of pediatric and adolescent gymnasts throughout their musculoskeletal injury recovery.

NCT ID: NCT05110092 Enrolling by invitation - Quality of Life Clinical Trials

Breathing-based Leg Resistance Exercise Improves Wound Healing, Blood Sugar and Quality of Life for Diabetic Foot Ulcers

Start date: December 14, 2016
Phase: N/A
Study type: Interventional

The purpose of the study was designed leg resistance training combined with breathing approach, and evaluated its effect on wound healing, blood sugar control and quality of life in type 2 diabetic patients with foot ulcers.

NCT ID: NCT05108909 Recruiting - Clinical trials for MTBI - Mild Traumatic Brain Injury

Rapid Diagnosis and Prognosis Recognition of Imaging and Biomarkers in Mild to Moderate Traumatic Brain Injury

Start date: September 1, 2021
Phase:
Study type: Observational

The investigators will carry out multi-center and large sample research based on the Chinese population, screen the optimal diagnostic and prognosis recognition biomarkers and analyze the diagnostic critical cutoff values in patients with mild to moderate traumatic brain injury, so as to provide a substantial basis for clinical diagnosis and prognosis recognition.

NCT ID: NCT05107752 Recruiting - PTSD Clinical Trials

Stellate Ganglion Block to Augment Trauma-focused Therapy Among Veterans With PTSD

Start date: January 3, 2022
Phase: Phase 2
Study type: Interventional

Our long-term goal is to improve clinical outcomes among patients receiving psychological treatment for posttraumatic stress disorder (PTSD). The primary objective of this project is to examine if stellate ganglion block (SGB) improves outcomes among military personnel and veterans receiving cognitive processing therapy (CPT), an empirically-supported psychological treatment for PTSD. To accomplish this objective, we will enroll adult military personnel and veterans with a current diagnosis of PTSD and/or subthreshold PTSD, provide CPT sessions over two weeks, administer SGB during or after CPT, and repeatedly assess key outcomes during follow-up.