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Wounds and Injuries clinical trials

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NCT ID: NCT06162130 Completed - Muscle Weakness Clinical Trials

Muscular Activations During Eccentric Quadriceps Exercises

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to investigate muscular activations during various quadriceps exercises commonly used in clinical settings.

NCT ID: NCT06159946 Completed - Clinical trials for Spinal Cord Injury Cervical

Access-H20 Faucet for Spinal Cord Injury

Start date: August 15, 2022
Phase: N/A
Study type: Interventional

The Phase I SBIR objective is to design, develop & demonstrate feasibility of Access-H2OTM, a sensor driven smart faucet to enable and empower independent drinking and grooming for individuals impacted by spinal cord injury (SCI). SCI severely impacts functional independence & ability to perform activities of daily living (ADLs). Greater function is typically lost with higher, more complete injuries. More specifically, those impacted above C5-C7 have impaired upper extremities, which limits the use of arms and hands for activities such as eating, drinking, and grooming. Functional access to water for these individuals becomes a key to increased independence and successful completion of ADLs. Therefore, commercialization of smart fountain faucets, which can automatically deliver water in target temperature, force, & nozzle setting for a specific ADL, has the potential to empower individuals with SCI for greater independence & and improved quality of life. Subjects with SCI and controls were recruited to test the functionality of the faucet which includes eye gaze, voice, and motion sensors to control the water stream for drinking, rinsing, and grooming.

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: NCT06146829 Completed - 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.

NCT ID: NCT06145789 Completed - Clinical trials for Spinal Cord Injuries

The Use of Standing Powered Wheelchairs in Spinal Cord Injury

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

The purpose of this study was to explore the experiences of standing powered wheelchair users with spinal cord injury.

NCT ID: NCT06137456 Completed - Clinical trials for Spinal Cord Injuries

First Report of a New Exoskeleton in Incomplete Spinal Cord Injury

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the effects of exoskeletal robotic therapy and conventional exercise therapy in incomplete spinal cord injury (SCI). The main questions it aims to answer are: - Is exoskeletal robotic therapy effective in improving functional ambulation in SCI? - Is exoskeletal robotic therapy effective in enhancing Activities of Daily Living in SCI? Participants treated with either: - Exoskeletal robotic therapy along with conventional exercise therapy, or - Only conventional exercise therapy.

NCT ID: NCT06137443 Completed - Clinical trials for Spinal Cord Injuries

Enhancing Balance and Mobility in Incomplete Spinal Cord Injury

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the effects of balance therapy with an overground gait trainer in incomplete spinal cord injury (SCI). The main questions it aims to answer are: - Is balance therapy with an overground gait trainer effective in improving functional ambulation in SCI? - Is balance therapy with an overground gait trainer effective in enhancing Activities of Daily Living in SCI? Participants treated with either: • Overground gait trainer along with conventional exercise therapy

NCT ID: NCT06135610 Completed - COVID-19 Clinical Trials

Social Determinants of Health in Patients With Penetrating Trauma Injuries Before and During the COVID-19 Pandemic

Start date: March 1, 2019
Phase:
Study type: Observational

Investigators report on the impact of the COVID-19 stay-at-home order concerning penetrating violence and its association within different socioeconomic regions within the county. The distribution and volume of violent offenses prior to the stay-at-home order was compared to during the stay-at-home order. This bears a crucial significance in our injury prevention and education efforts within our community.

NCT ID: NCT06126549 Completed - Clinical trials for Acquired Brain Injury

Comparison of Two Interventions for Caregivers of Patients With Acquired Brain Injury

Start date: February 16, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare effectiveness of two interventions for family caregivers of patients with acquired brain injury who are transitioning home after inpatient rehabilitation. The main question it aims to answer is whether these interventions reduce caregiver stress and burden, compared to usual care. Secondary effects include the impact on caregivers' depressive symptoms and perceived self-efficacy as a caregiver. The study will also try to determine if caregivers will engage in these interventions during the acute (inpatient rehabilitation) stage of injury. Participants in the study are family members of the ABI patient, aged 18 year or older, who will be responsible for the patient's care and supervision once discharged home from inpatient rehabilitation. The two interventions, one clinician-led and one peer-led, will be compared to usual care.

NCT ID: NCT06118177 Completed - Gingival Recession Clinical Trials

Ultrasonographic Assessment of Palatal Wound Healing

Start date: September 5, 2022
Phase:
Study type: Observational [Patient Registry]

Palatal-tissue harvesting is a routinely performed procedure in periodontal plastic surgery. Subepithelial connective tissue graft (sCTG) is considered the gold standard in root coverage. However, over the years, several materials have been attempted to accelerate wound healing and to decrease the post-operative patient discomfort and pain, which are considered the most common disadvantages of tissue harvesting from the palate. Reharvesting from the same region could be necessary in some complicated gingical recessions. For this reason, patients may face long treatment times due to recovery periods of the palate between surgeries. Platelet-rich fibrin (PRF) which has 3-dimensional fibrin matrix structure contributes to regeneration of surgical wounds by releasing growth factors for 10-14 days and showing angiogenic properties. In medicine and dentistry, ultrasonography (USG) method can be used to measure tissue thickness, vascularization, elasticity and blood flow. USG, as a non-invasive method, can provide objective data in evaluating the effects of surgical techniques and biomaterials used on soft tissue healing dynamics and tissue perfusion. The investigators hypothesised that leukocyte rich PRF (L-PRF) application to the palatal area after sCTG harvesting could increase palatal tissue thickness and vascularity throughout 3-month follow-up period compared to the controls. Therefore, in this study, the investigators aimed to evaluate the effects of the L-PRF membrane on soft tissue donor site healing after harvesting sCTG in terms of wound healing dynamics using USG method.