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Wounds and Injuries clinical trials

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NCT ID: NCT05022095 Completed - Clinical trials for SCI - Spinal Cord Injury

"Validated Language Transfer of the Spinal Cord Injury-Spasticity Evaluation Tool to German Language"

SCI-SETde
Start date: August 30, 2021
Phase:
Study type: Observational

To better depict the full range of spasticity after Spinal Cord Injury (SCI) there is a need to take into account the patients perspective and their experiences during daily life. In 2007 the Spinal Cord Injury-Spasticity Evaluation Tool (SCI-SET) was created and validated. This specific questionnaire addresses the influence of spasticity on the daily life of SCI patients and takes into account negative as well as positive effects of spasticity to fulfill certain tasks. Until now this questionnaire is only available in english, turkish and persian language. Therefore, the investigators translated and culturally adapted this questionnaire and within this study this questionnaire shall be validated in a small cohort of SCI patients. The patients will fill in several different questionnaires at a first meeting and one week later the SCI-SETde questionnaire again to evaluate test-retest properties. Recruiting will happen completely at the Swiss Paraplegic Centre Nottwil, Switzerland.

NCT ID: NCT05009576 Completed - Wound Healing Clinical Trials

Comparative Study Using Negative Pressure Dressing With & Without Silver Alginate to Promote Healing in Chronic Wounds.

Start date: December 17, 2020
Phase: N/A
Study type: Interventional

The randomized control trial will be conducted in the Department of Plastic and Reconstructive Surgery at Dr. Ruth K.M. Pfau Civil Hospital Karachi.General population admitted in Civil Hospital Karachi, for wound coverage with skin grafting meetimg inclusion criteria will be included.

NCT ID: NCT05007366 Completed - Knee Osteoarthritis Clinical Trials

Optimizing Gait Biomechanics for Posttraumatic Osteoarthritis Prevention

Start date: August 5, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to report the feasibility and determine the initial effects of 18 sessions of real-time gait biofeedback delivered over a 6-week period on retention and transfer of normalized gait biomechanics and improvements in indicators of early post-traumatic osteoarthritis development in those with an anterior cruciate ligament reconstruction (ACLR) at 6 and 8-week posttests.

NCT ID: NCT05006820 Completed - Sports Injury Clinical Trials

Epidemiology of Roller Hockey Related Injuries.

Start date: July 15, 2021
Phase:
Study type: Observational

Roller Hockey is a sport played on a 40*20 metres rink characterized by combined periods of high intensity and short breaks, there´s a lack of epidemiological studies in this field. In line with the well-established model of sports injury prevention research proffered by van Mechelen, the first stage in this process is establishing the extent of the problem i.e. injury incidence, severity and burden. Through an online survey filled by semiprofessional athletes, it is posible to obtain all this important information. This way, it will be possible to fulfill a gap in the literature and take action in the near future in order to reduce the prevalence of injuries in this sport.

NCT ID: NCT05003999 Completed - Clinical trials for Spinal Cord Injuries

Time Needed to Perform Intermittent Catheterization in Adults With Spinal Cord Injuries

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

This study investigates the burden of intermittent catheterization in adult individuals with neurogenic lower urinary tract dysfunction (NLUTD) following spinal cord injury (SCI). Individuals will be recruited to compare two types of catheters. Each participant will use a non-hydrophilic catheter at one time point and a hydrophilic catheter at a different time point to perform intermittent catheterization. The order that participants use either a non-hydrophilic or a hydrophilic catheter will be determined randomly. The purpose of the study is to provide evidence for time spent on bladder management (performing intermittent catheterization) as well as consumer satisfaction on using both catheters.

NCT ID: NCT04999397 Completed - Clinical trials for Penetrating Cardiac Trauma

Penetrating Cardiac Injuries: Outcome of Treatment From a Level 1 Trauma Centre in South

Start date: January 1, 2016
Phase:
Study type: Observational

Retrospective observational study design auditing the outcomes of cardiac injuries in a single centre

NCT ID: NCT04999163 Completed - Acute Kidney Injury Clinical Trials

Aortix Therapy for Perioperative Reduction of Kidney Injury

A Priori
Start date: June 5, 2022
Phase: N/A
Study type: Interventional

The study is a prospective, non-randomized feasibility study to evaluate the safety and performance of providing support with the Aortix System to patients at heightened risk of acute kidney injury (AKI) undergoing cardiovascular surgery.

NCT ID: NCT04997915 Completed - Critical Illness Clinical Trials

Acute Kidney Injury in Coronavirus Disease-19 (COVID-19) Patients Admitted to the Intensive Care Unit (ICU)

COVID-AKI-B
Start date: February 1, 2020
Phase:
Study type: Observational

The aim of this study is to evaluate the rate and outcomes of COVID-19 associated acute kidney injury (AKI) and use of kidney replacement therapy (KRT) in critically ill COVID-19 patients in ICUs in several large hospitals in Flanders, the northern region of Belgium. We will also explore the associations between several baseline risk factors for AKI, therapeutic strategies and COVID-19 related clinical signs and the occurrence of AKI and use of KRT.

NCT ID: NCT04992351 Completed - Anesthesia, Local Clinical Trials

Wide-awake Local Anesthesia and no Tourniquet (WALANT) in Plastic Surgery

Start date: June 1, 2019
Phase:
Study type: Observational [Patient Registry]

Wide-awake local anesthesia no tourniquet (WALANT) was proposed and performed in hand operations. Aim of this study is to present the use of WALANT in operations performed on the upper and lower limbs, evaluate its efficacy in terms of feasibility, total operation time, total operating room time, bleeding, patient discomfort and satisfaction and control for potential drawbacks. The hypothesis is that WALANT is a viable option in common operations performed by plastic surgeons on the upper and lower limbs.

NCT ID: NCT04989582 Completed - Clinical trials for Nurses Who Have Experienced Trauma

Effectiveness of a Nursing Intervention for Nurses Have Experienced Trauma: a Study Based on Swanson's Caring Theory

Start date: May 7, 2020
Phase: N/A
Study type: Interventional

This study aimed to (1) develop an internet-based psychiatric nursing intervention, based on Swanson's theory of caring, and (2) examine its effects on functional health, resilience, social support, post-traumatic stress, depression, and anxiety. This study was a randomized clinical trial(RCT) study with repeated measures to identify the effectiveness of an internet-based psychiatric nursing intervention. Participants were evaluated at the following time points: pre-test (pre), post-test (post-test 1, immediately after intervention), and follow-up (post-test 2, one month after the intervention) to assess the sustainability of the internet-based psychiatric nursing intervention. Of the 112 women who enrolled in the study, 10 dropped out before post-test 1, resulting in 102 participants who completed all interventions and surveys.