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Wounds and Injuries clinical trials

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NCT ID: NCT03888703 Completed - Burns Clinical Trials

The Use of Fractional Ablative CO2 Laser vs Control on Acute Traumatic Injuries to Prevent Scar Formation

Start date: May 4, 2015
Phase: N/A
Study type: Interventional

Surgical standard for treating traumatic burn injury scarring is to wait one year following the initial assault prior to beginning treatment. This study investigates the use of fractional ablative CO2 laser when begun within 3 months of a traumatic burn injury and it's impact on scar formation compared to the control. We hypothesized that early intervention would substantially mitigate the formation of scar tissue and help restore more normal appearing skin.

NCT ID: NCT03887299 Completed - Clinical trials for Cesarean Section Complications

Antimicrobial Dressing Versus Standard Dressing in Obese Women Undergoing Cesarean Delivery

Start date: April 18, 2019
Phase: Phase 4
Study type: Interventional

This will be an open label pilot randomized controlled clinical trial. Women undergoing cesarean delivery will be randomized to have standard wound dressing care or chlorohexidine gluconate (CHG) impregnated wound dressing (ReliaTectâ„¢ Post-Op Dressing).

NCT ID: NCT03886610 Completed - Clinical trials for Spinal Cord Injuries

Association of Quantitative and Functional Imaging With Clinical Outcome After Spinal Cord Injury

Start date: March 27, 2019
Phase:
Study type: Observational

The overall study aim is to provide additional magnetic resonance imaging parameters of the cervical spinal cord, brainstem and brain and a better understanding of changes after spinal cord injury (SCI) and to define new magnetic resonance (MR) biomarkers to correlate with sensomotoric functioning and clinical outcome.

NCT ID: NCT03883230 Completed - Diabetic Foot Clinical Trials

Wound Infection Detection Evaluation, WIDE

WIDE
Start date: July 27, 2017
Phase:
Study type: Observational

Chronic wounds, such as diabetic foot ulcers, place a huge burden on healthcare systems and can lead to complications with high morbidity, particularly if the wound if infected. In parallel, there is pressure to reduce the use of antibiotics in order to minimise the risk of antimicrobial resistance. The Glycologic wound detection kit (GLYWD) is a point-of-care test, designed to provide guidance to clinical staff as to whether a chronic wound is infected or not. In this prospective cohort study the premise of this mode-of-action is evaluated. GLYWD will be applied in conjunction with clinical opinion and microbiological testing to determine if there is concordance between the different diagnostic approaches, and if applicable how they may differ in certain patients' wounds.

NCT ID: NCT03882658 Completed - Acute Kidney Injury Clinical Trials

Preoperative Serum Albumin and Duration of Intraoperative Hypotension on Postoperative Acute Kidney Injury

Start date: January 10, 2018
Phase:
Study type: Observational

Acute kidney injury is one of major adverse postoperative complications. research about postoperative acute kidney injury conclude that low preoperative albumin and intraoperative hypotension is associated to postoperative acute kidney injury. However, due to ethic issue and nonlinear realtionship between these factors and postoperative acute kidney injury, the exact threshold of these two risk factors were not be able to identified. The research tried to locate the exact threshold with implementation of penalized splines by generalized additive model.

NCT ID: NCT03880331 Completed - Wound Heal Clinical Trials

Prospective Randomized Clinical Trial Comparing Outcomes of Secondary Intention Wound Care Methods

Start date: December 3, 2019
Phase: N/A
Study type: Interventional

This is a randomized controlled trial which is designed to determine whether aggressive and frequent debridement of an acute post-surgical wound shortens healing time.

NCT ID: NCT03879070 Completed - Clinical trials for Acquired Brain Injury

Experimentation of an Ankle Mobilization Device for the Rehabilitation of Patients With Acquired Brain Injuries.

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

The proposed clinical investigation plan is a randomized controlled pivotal study with 2 parallel groups, has a total duration of two years. For the study, 30 pediatric patients suffering from acquired brain injury will be recruited at the Scientific institute Eugenio Medea. The primary aim of this study is to assess the clinical benefit of using an ankle mobilization device for the rehabilitation of pediatric patients with acquired brain injuries, on its clinical performance and its risks, and on its safety. The efficacy of the treatment will be evaluated in terms of ankle range of motion (primary outcome). The effects of the treatment on musculoskeletal plasticity will be studied using an isokinetic machine and functional magnetic resonance imaging will provide information on variations of reactivity in the motor cortical network. Ease of use, safety and usability of the device will also be evaluated.

NCT ID: NCT03877133 Completed - Clinical trials for Liver Transplant; Complications

Association of Intraoperative Renal Regional Oxygen Saturation and Acute Kidney Injury

Start date: March 11, 2019
Phase: N/A
Study type: Interventional

This study is a prospective observational study of a single cohort of the patients who will undergo a scheduled living donor liver transplantation. The investigators attempt to evaluate the association of intraoperative renal regional oxygen saturation and acute kidney injury in patients undergoing living donor liver transplantation. Near-infrared spectroscopy sensor will be attached to the skin near bilateral kidney areas in all patients and renal regional oxygen saturation will be monitored during the operation. Renal regional oxygen saturation (rSO2) of the patients who developed acute kidney injury postoperatively will be compared with rSO2 of the patients who did not.

NCT ID: NCT03876743 Completed - Knee Injuries Clinical Trials

Opiates Prescribing for Knee Arthroscopies and ACL Reconstruction

Start date: March 26, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if opiates are required to achieve adequate analgesia after knee arthroscopy and ACL reconstruction in outpatient surgery. The investigators hypothesize that patients are frequently prescribed more opiates than are needed after surgery, resulting in excess medications that are at risk for misuse, diversion and contribution to the opioid epidemic.

NCT ID: NCT03875066 Completed - Clinical trials for Spinal Cord Injuries

Immediate Effects of Stepping Training Using External Feedback in Spinal Cord Injury Patients

Start date: April 19, 2017
Phase: N/A
Study type: Interventional

- Does stepping training with or without external feedback change functional ability of ambulatory patients with iSCI immediately after training? - Are there significant differences between the immediate effects of stepping training with or without external feedback in ambulatory patients with iSCI?